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As a Clinical Research Associate (CRA), you&#39;ll collaborate with sites, data-driven insights, and focus on activities that truly impact study quality, patient safety, and success of the trial.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities, and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP, and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient.</li>\n<li>Assesses factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site.</li>\n<li>Conducts Source Document Review of appropriate site source documents and medical records.</li>\n<li>Verifies required clinical data entered in the case report form (CRF) is accurate and complete.</li>\n<li>Applies query resolution techniques remotely and on-site, and provides guidance to site staff as necessary.</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness, and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents.</li>\n<li>Supports subject/patient recruitment, retention, and awareness strategies.</li>\n<li>Enters data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution.</li>\n<li>May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience.</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.</li>\n<li>Previous monitoring experience in Germany, preferably in oncology.</li>\n<li>Experience in risk-based monitoring is a plus.</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies.</li>\n<li>Excellent communication, presentation, and interpersonal skills.</li>\n<li>Fluency in German and English.</li>\n<li>Location in north-east Germany.</li>\n<li>Ability to manage required travel of up to 75% on a regular basis.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/Clinical-Research-Associate_25111958-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/Clinical-Research-Associate_25111958-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","monitoring","risk-based monitoring","German","English","computer skills"],"x-skills-preferred":["oncology"],"datePosted":"2026-10-28T08:49:34.082Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, monitoring, risk-based monitoring, German, English, computer skills, oncology"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_98017f69-ace"},"title":"CRA II","description":"<p>Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. The Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions they shape.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site.</li>\n<li>Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes, conducts Source Document Review of appropriate site source documents and medical records.</li>\n<li>May perform investigational product (IP) inventory, reconciliation and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.</li>\n<li>For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.</li>\n<li>May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client-Hangzhou/CRA-II---Hangzhou_25112539","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client-Hangzhou/CRA-II---Hangzhou_25112539","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T08:46:09.423Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b7940805-872"},"title":"Senior Project Manager, Laboratory","description":"<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>\n<p>As a Senior Project Manager, Laboratory at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will oversee clinical laboratory operations workstreams, ensuring deliverables meet quality and timeline expectations. 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function</li>\n<li>Manage staff in accordance with the organisation&#39;s policies and applicable regulations</li>\n</ul>\n<p><strong>Responsibilities</strong> include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems; and approving actions on human resources matters.</p>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor&#39;s Degree or educational equivalent required</li>\n<li>3-4 years of relevant experience, including 1 year in a leadership capacity and/or equivalent combination of education, training, and experience</li>\n<li>In-depth knowledge of CTM packaging procedures</li>\n<li>Working knowledge of applicable hazardous goods shipping regulations</li>\n<li>Knowledge of applicable human resources policies and procedures</li>\n<li>Effective leadership skills</li>\n<li>Excellent customer service skills</li>\n<li>Good written and verbal communication skills</li>\n<li>Good word processing skills</li>\n<li>Excellent organisational skills</li>\n<li>Attention to detail</li>\n<li>Ability to work in a fast-paced environment</li>\n<li>Ability to establish and maintain effective working relationships with co-workers, managers, and clients</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/Supv--Clinical-Trial-Mtls_R1269903","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Q2 Solutions","sameAs":"https://q2labsolutions.com/careers","logo":"https://logos.yubhub.co/q2labsolutions.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/Supv--Clinical-Trial-Mtls_R1269903","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical 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requirements.</li>\n<li>Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.</li>\n<li>Collaborate and liaise with study team members for project execution support as appropriate.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s Degree in scientific discipline or health care preferred.</li>\n<li>At least 2 years of on-site monitoring experience.</li>\n<li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.</li>\n<li>Good therapeutic and protocol knowledge as provided in company training.</li>\n<li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where 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The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff, providing recommendations regarding site-specific actions</li>\n<li>Verify process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>Perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution</li>\n<li>Understand project scope, budgets, and timelines, and manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>Act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to embrace new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/AUS-Remote/CRA-II--SCRA--NSW--VIC--QLD-_25112760","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/AUS-Remote/CRA-II--SCRA--NSW--VIC--QLD-_25112760","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T05:52:30.616Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b193a598-fb6"},"title":"Sr CRA - Beijing","description":"<p>Syneos Health is seeking a Senior Clinical Research Associate (CRA) to join their team in Beijing. As a Sr CRA, you will play a critical role in ensuring the quality and compliance of clinical research studies.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices</li>\n<li>Develop and implement tools, procedures, and processes to ensure quality monitoring</li>\n<li>Contribute to the design, implementation, and delivery of processes, programs, and policies</li>\n<li>Manage and direct the work of lower-level professionals or manage processes and programs</li>\n<li>Ensure accurate and timely documentation and reporting of clinical trial data</li>\n<li>Collaborate with cross-functional teams to support clinical trial activities</li>\n<li>Identify and resolve issues related to clinical trial conduct and data integrity</li>\n<li>Provide training and mentorship to junior staff members</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a related field</li>\n<li>Minimum of 3-5 years of experience in clinical research or a related field</li>\n<li>In-depth knowledge of clinical trial processes and regulations</li>\n<li>Strong analytical and problem-solving skills</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and as part of a team</li>\n</ul>\n<p><strong>Certifications</strong></p>\n<ul>\n<li>Certified Clinical Research Professional (CCRP) or equivalent certification preferred</li>\n</ul>\n<p><strong>Necessary Skills</strong></p>\n<ul>\n<li>Proficiency in clinical trial management systems and software</li>\n<li>Strong organizational and time management skills</li>\n<li>Attention to detail and accuracy</li>\n<li>Ability to manage multiple projects and priorities simultaneously</li>\n<li>Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/CRA_25000353","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/CRA_25000353","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial management","Good Clinical Practice","regulatory compliance","data analysis","communication"],"x-skills-preferred":["Certified Clinical Research Professional","clinical trial management systems"],"datePosted":"2026-10-28T05:46:22.044Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Beijing"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical trial management, Good Clinical Practice, regulatory compliance, data analysis, communication, Certified Clinical Research Professional, clinical trial management systems"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9eaf7065-f43"},"title":"PMS CTM/PM for FSP BU in South Korea","description":"<p>Syneos Health is seeking a PMS CTM/PM for FSP BU in South Korea.</p>\n<p>As a Project Manager, you will oversee interdisciplinary clinical research studies and ensure compliance with GCP, relevant SOP&#39;s, and regulatory requirements.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Managing projects and ensuring timely study launch, conduct, and closeout</li>\n<li>Acting as primary liaison between the Company and the Customer</li>\n<li>Leading project teams to ensure quality, timelines, and budget management</li>\n<li>Coordinating activities and deliverables of study conduct partners</li>\n<li>Ensuring studies are conducted in compliance with GCP, relevant SOP&#39;s, and regulatory requirements</li>\n<li>Maintaining study information on various databases and systems</li>\n<li>Developing contingency planning and risk mitigation strategies</li>\n<li>Building strong relationships with clients to generate new business</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in life sciences, medicine, pharmacy, nursing, or equivalent</li>\n<li>Clinical research organization experience and relevant therapeutic experience preferred</li>\n<li>Strong knowledge of Good Clinical Practice/ICH guidelines and regulatory requirements</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to travel approximately 25%</li>\n</ul>\n<p>Syneos Health offers a dynamic work environment, opportunities for career development, and a Total Self culture that encourages authenticity and diversity.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Remote/PMS-CTM-PM-for-FSP-BU-in-South-Korea_25112987","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Remote/PMS-CTM-PM-for-FSP-BU-in-South-Korea_25112987","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","clinical research","project management","regulatory compliance","interpersonal skills"],"x-skills-preferred":["clinical research organization experience","therapeutic area expertise","new technologies"],"datePosted":"2026-10-28T05:18:23.387Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, clinical research, project management, regulatory compliance, interpersonal skills, clinical research organization experience, therapeutic area expertise, new technologies"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_90ca47c8-152"},"title":"CRA II - Beijing","description":"<p>Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes, Conducts Source Document Review of appropriate site source documents and medical records, Verifies required clinical data entered in the case report form (CRF) is accurate and complete.</li>\n<li>May perform investigational product (IP) inventory, reconciliation and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.</li>\n<li>For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.</li>\n<li>May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA).</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/CRA-II---Beijing_25111939","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/CRA-II---Beijing_25111939","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T04:21:27.696Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Beijing"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_f88667d2-92f"},"title":"CRA II- SCRA","description":"<p>Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. They partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes.</li>\n<li>May perform investigational product (IP) inventory, reconciliation and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.</li>\n<li>For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.</li>\n<li>May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/AUS-Remote/SAS-I-II_25111776-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/AUS-Remote/SAS-I-II_25111776-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T04:12:33.805Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_f24a41c5-307"},"title":"Call Center Nurse","description":"<p>The call center nurse will serve as the virtual study coordinator for Principal Investigators (PIs) and patients participating in pregnancy registries and other observational trials.</p>\n<p>As a call center nurse, you will be the primary contact for patients and healthcare professionals (HCPs) participating in a registry, facilitating completion of protocol-specific tasks remotely using the telephone, email, fax, and various portals.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Providing information and follow-up to incoming calls and emails per project direction</li>\n<li>Administering informed consent verbally or online</li>\n<li>Following up with patients and/or HCPs per protocol</li>\n<li>Collecting and entering data in the study electronic data capture system (EDC) per protocol</li>\n<li>Recognising and escalating any adverse events (AEs) or serious adverse events (SAEs) according to protocol</li>\n<li>Resolving any data queries</li>\n<li>Maintaining investigator site files as necessary</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in Nursing Science (BSN) with 2+ years of experience</li>\n<li>Obstetrics and Gynecology (OBGYN) experience is a plus</li>\n<li>Previous experience in clinical trials or real-world (phase 4) observational research</li>\n<li>Fluency in English</li>\n<li>Working knowledge of Good Clinical Practice (GCP) principles, with certification required</li>\n<li>Proficiency in MS Windows and Office applications, such as Excel, Outlook, and Word</li>\n<li>Excellent interpersonal skills</li>\n<li>Attention to detail and ability to establish effective working relationships</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Pasig-City-Philippines/System-Support-Analyst_R1358012","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Pasig-City-Philippines/System-Support-Analyst_R1358012","x-work-arrangement":"remote","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","MS Windows","Office applications","English"],"x-skills-preferred":["OBGYN experience","clinical trials experience"],"datePosted":"2026-10-28T04:08:34.881Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, MS Windows, Office applications, English, OBGYN experience, clinical trials experience"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c346246f-86c"},"title":"Project Manager, Oncology - Sponsor Dedicated","description":"<p>Syneos Health is seeking a Project Manager, Oncology - Sponsor Dedicated. As a Project Manager, you will oversee interdisciplinary clinical research studies and ensure compliance with GCP, relevant SOP&#39;s, and regulatory requirements.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Manage a project as a project manager overseeing interdisciplinary clinical research studies and ensure compliance with GCP, relevant SOP&#39;s, and regulatory requirements.</li>\n<li>Act as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer&#39;s and the Company&#39;s contractual agreement.</li>\n<li>Lead project team to ensure quality, timelines, and budget management.</li>\n<li>Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.</li>\n<li>Ensure studies are conducted in compliance with GCP, relevant SOP&#39;s, and regulatory requirements.</li>\n<li>Develop strong relationships with current clients to generate new and/or add-on business for the future.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience.</li>\n<li>Clinical research organization (CRO) and relevant therapeutic experience preferred.</li>\n<li>Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.</li>\n<li>Strong organizational skills.</li>\n<li>Excellent communication, presentation, interpersonal skills, both written and spoken.</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Company car or car allowance</li>\n<li>Health benefits to include Medical, Dental, and Vision</li>\n<li>Company match 401k</li>\n<li>Eligibility to participate in Employee Stock Purchase Plan</li>\n<li>Eligibility to earn commissions/bonus based on company and individual performance</li>\n<li>Flexible paid time off (PTO) and sick time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-Remote/Project-Manager--Oncology---Sponsor-Dedicated_25111820","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-Remote/Project-Manager--Oncology---Sponsor-Dedicated_25111820","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"The base salary range represents the anticipated low and high of the Syneos Health range for this position.","x-skills-required":["Good Clinical Practice","ICH guidelines","life sciences","Medicine","Pharmacy","Nursing","clinical research","project management"],"x-skills-preferred":["Clinical research organization (CRO)","relevant therapeutic experience","strong organizational skills","excellent communication skills"],"datePosted":"2026-10-28T04:01:44.844Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH guidelines, life sciences, Medicine, Pharmacy, Nursing, clinical research, project management, Clinical research organization (CRO), relevant therapeutic experience, strong organizational skills, excellent communication skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_759f9dd1-6f7"},"title":"Clinical Supply Chain Manager","description":"<p>Syneos Health is seeking a Clinical Supply Chain Manager to lead the operational and financial aspects of clinical trial supplies management during the complete project life cycle. The successful candidate will provide customer-focused leadership, liaising with customers, vendors, and investigative sites to manage Clinical Trial Supplies deliverables.</p>\n<p><strong>Core Responsibilities</strong></p>\n<ul>\n<li>Manage clinical trial supplies for assigned studies and ensure compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), relevant standard operating procedures (SOPs), and regulatory requirements</li>\n<li>Be accountable for the operational delivery and financial performance of services assigned to the Clinical Supplies team</li>\n<li>Liaise with the Supply Chain Logistics Coordinator for IoR/EoR services as required</li>\n<li>Lead the identification of and contracting with approved Clinical Trial Supplies related vendors, as necessary</li>\n<li>Provide vendor management, inclusive of ensuring key Clinical Trial Supplies deliverables are met and financial parameters of contracts are upheld</li>\n<li>Define supplies requirements in collaboration with client packaging and distribution vendors and the Project Lead (PL)</li>\n<li>Provide oversight for the creation, implementation, and maintenance of drug and supply distribution plans</li>\n<li>Be accountable for maintenance of project information on a variety of databases and systems</li>\n<li>Oversee the inventory, supply, and re-supply plans for subject kits and/or study medication required for the duration of a study and provide relevant reports for customers and management</li>\n<li>Provide oversight for development and implementation of project plans in accordance with Controlled Documents and ensure proper archival of records in Trial Master Files to ensure inspection readiness</li>\n<li>Develop contingency planning and risk mitigation strategies to ensure successful provision of all required clinical trial supplies</li>\n<li>Participate in bid defense meetings to demonstrate overall capabilities of the Clinical Trial Supplies Management team and specific strategies for management of clinical trial supplies logistics for new business opportunities</li>\n<li>Develop strong relationships with current and potential customers to ensure satisfaction and identify new business opportunities</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing, or a related field</li>\n<li>Prior experience in a contract research organization (CRO), pharmaceutical, or biotechnology company in project management or clinical trial supplies management</li>\n<li>Strong knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practices, and other applicable regulatory requirements</li>\n<li>Strong organizational skills</li>\n<li>Strong ability to manage time and work independently</li>\n<li>Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade</li>\n<li>Flexibility and ability to handle multiple tasks to meet deadlines while delivering high-quality work in a dynamic environment</li>\n<li>High level of competency in English language</li>\n<li>Proficiency with MS Office Applications</li>\n<li>Ability to travel as necessary (up to 25%)</li>\n</ul>\n<p><strong>Benefits</strong> Syneos Health offers a range of benefits, including career development and progression, supportive and engaged line management, technical and therapeutic area training, peer recognition, and total rewards program.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Remote/Clinical-Supply-Chain-Manager_25110166-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Remote/Clinical-Supply-Chain-Manager_25110166-1","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","Good Manufacturing Practices","ICH guidelines","MS Office Applications","Life Sciences","Medicine","Pharmacy","Nursing"],"x-skills-preferred":[],"datePosted":"2026-10-28T04:01:43.516Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Logistics & Supply Chain","industry":"Healthcare","skills":"Good Clinical Practice, Good Manufacturing Practices, ICH guidelines, MS Office Applications, Life Sciences, Medicine, Pharmacy, Nursing"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_70b7c36a-e48"},"title":"Global Senior Project Specialist (Sponsor Dedicated) Germany","description":"<p>Syneos Health is seeking a Global Senior Project Specialist (Sponsor Dedicated) to join their team in Germany.</p>\n<p>The successful candidate will be responsible for setting up, maintaining, and closing out project files and study information on various databases and systems.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Setting up, maintaining, and closing out project files and study information</li>\n<li>Attending and participating in internal and external meetings, preparing and distributing meeting minutes and action items</li>\n<li>Maintaining timely and effective communication among team members and site staff</li>\n<li>Providing administrative support to Project Leads and functional leads</li>\n<li>Ensuring all study documents are archived based on guidelines and policy</li>\n<li>Providing support for quality assurance activities, including preparation for audits and internal review</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>Associate&#39;s degree in life sciences, medicine, pharmacy, nursing, or a related field</li>\n<li>Knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements</li>\n<li>Previous experience as a Project Specialist within a CRO/pharma company</li>\n<li>Strong organizational skills</li>\n<li>Global trial experience</li>\n<li>Ability to manage time and work independently</li>\n<li>High proficiency with MS Office Applications</li>\n<li>Strong communication, presentation, and interpersonal skills</li>\n</ul>\n<p>Syneos Health offers a range of benefits, including career development and progression, supportive line management, technical and therapeutic area training, and a total rewards program.</p>\n<p>The company is committed to its Total Self culture, which encourages employees to be themselves and provides a supportive and inclusive work environment.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/Global-Senior-Project-Specialist--Sponsor-Dedicated--Germany_25111704","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/Global-Senior-Project-Specialist--Sponsor-Dedicated--Germany_25111704","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH guidelines","MS Office Applications","organizational skills","communication skills","interpersonal skills"],"x-skills-preferred":["global trial experience","travel experience"],"datePosted":"2026-10-28T03:49:18.304Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH guidelines, MS Office Applications, organizational skills, communication skills, interpersonal skills, global trial experience, travel experience"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_fff075a7-ddf"},"title":"CRA II - Sponsor Dedicated - West Coast","description":"<p>Syneos Health is seeking a CRA II - Sponsor Dedicated - West Coast.</p>\n<p>Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.</p>\n<p>The Clinical Development model brings the customer and the patient to the center of everything that they do. They are continuously looking for ways to simplify and streamline their work to not only make Syneos Health easier to work with, but to make them easier to work for.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site.</li>\n<li>Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes.</li>\n<li>May perform investigational product (IP) inventory, reconciliation and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.</li>\n<li>For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.</li>\n<li>May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p><strong>Benefits</strong></p>\n<ul>\n<li>Company car or car allowance</li>\n<li>Health benefits to include Medical, Dental and Vision</li>\n<li>Company match 401k</li>\n<li>Eligibility to participate in Employee Stock Purchase Plan</li>\n<li>Eligibility to earn commissions/bonus based on company and individual performance</li>\n<li>Flexible paid time off (PTO) and sick time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-OR-Remote/CRA-II---Sponsor-Dedicated---West-Coast_25111754","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-OR-Remote/CRA-II---Sponsor-Dedicated---West-Coast_25111754","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$base salary range represents the anticipated low and high of the Syneos Health range for this position","x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T03:49:15.719Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_606941b3-b76"},"title":"Sponsor Dedicated CRA II/Sr CRA I/II - 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69,000.00 EUR, excluding any additional benefits and allowances.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ITA-Remote/Sponsor-Dedicated-CRA-II-Sr-CRA-I-II---Home-Based-ITA_25111710","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ITA-Remote/Sponsor-Dedicated-CRA-II-Sr-CRA-I-II---Home-Based-ITA_25111710","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"45,000.00 EUR - 69,000.00 EUR","x-skills-required":["Good Clinical Practice","ICH Guidelines","Risk-Based Monitoring","Clinical Monitoring","Site Management"],"x-skills-preferred":["Oncology monitoring","Phase I experience"],"datePosted":"2026-10-28T03:49:13.658Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, Risk-Based Monitoring, Clinical Monitoring, Site Management, Oncology monitoring, Phase I experience","baseSalary":{"@type":"MonetaryAmount","currency":"EUR","value":{"@type":"QuantitativeValue","minValue":45000,"maxValue":69000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_03423ebd-30e"},"title":"CRA II (client dedicated)","description":"<p>Syneos Health is seeking an experienced CRA to join their team. 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You will ensure regulatory, ICH-GCP, and protocol compliance, and use your judgment and experience to evaluate site performance and provide recommendations.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Ensure regulatory, ICH-GCP, and protocol compliance</li>\n<li>Evaluate site performance and provide recommendations</li>\n<li>Verify informed consent process and document confidentiality</li>\n<li>Assess site processes and conduct source document reviews</li>\n<li>Apply query resolution techniques and provide guidance to site staff</li>\n<li>Manage investigational product inventory and reconciliation</li>\n<li>Review Investigator Site File and reconcile contents with Trial Master File</li>\n<li>Document activities and support subject recruitment and retention</li>\n<li>Understand project scope, budgets, and timelines</li>\n<li>Adapt to changing priorities and achieve goals</li>\n<li>Act as primary liaison with study site personnel</li>\n<li>Prepare for and attend Investigator Meetings and sponsor face-to-face meetings</li>\n<li>Provide guidance on audit readiness standards</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to adapt to new technologies</li>\n<li>Fluency in German and English</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Location in South-West Germany, with ability to support Swiss sites</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/CRA-II--client-dedicated-_25113082","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/CRA-II--client-dedicated-_25113082","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory compliance","site management","clinical monitoring","German","English"],"x-skills-preferred":[],"datePosted":"2026-10-28T03:40:20.281Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory compliance, site management, clinical monitoring, German, English"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_5fb79557-dc7"},"title":"CRA II / Snr CRA - Multi Sponsor - Oncology","description":"<p>Syneos Health is seeking a CRA II / Snr CRA - Multi Sponsor - Oncology.</p>\n<p>The Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions they shape.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient.</li>\n<li>Assesses factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site.</li>\n<li>Conducts Source Document Review of site source documents and medical records.</li>\n<li>Verifies required clinical data entered in the case report form (CRF) is accurate and complete.</li>\n<li>Applies query resolution techniques remotely and on-site, and provides guidance to site staff as necessary.</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness, and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents.</li>\n<li>Supports subject/patient recruitment, retention, and awareness strategies.</li>\n<li>Enters data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution.</li>\n<li>May act as primary liaison with study site personnel or in collaboration with Central Monitoring Associate.</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience.</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies.</li>\n<li>Excellent communication, presentation, and interpersonal skills.</li>\n<li>Ability to manage required travel of up to 75% on a regular basis.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Bucharest-Hybrid/CRA-II---ROU_25110093","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Bucharest-Hybrid/CRA-II---ROU_25110093","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T03:25:07.349Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d81a25cd-c46"},"title":"Clinical Trial Manager","description":"<p>Syneos Health is seeking a Clinical Trial Manager to join their Clinical Solutions team. The successful candidate will be responsible for managing clinical trials from Phase 1 to Phase 4, ensuring compliance with regulations, and delivering high-quality results.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Manage clinical trials from initiation to close-out</li>\n<li>Ensure compliance with regulations, GCP, and protocol</li>\n<li>Coordinate with cross-functional teams, including investigators, research subjects, and client teams</li>\n<li>Develop and implement risk mitigation strategies</li>\n<li>Oversee site management, clinical monitoring, and central monitoring deliverables</li>\n<li>Review and provide feedback on study plans, budgets, and protocols</li>\n<li>Identify and escalate risks to clinical trial management deliverables</li>\n<li>Collaborate with other functional leaders to coordinate delivery handoffs and meet study milestones</li>\n<li>Develop and maintain clinical study tools and templates</li>\n<li>Provide training to study teams on protocol specifics, CRF completion, and Sponsor SOPs</li>\n<li>Oversee resourcing allocations for CRAs and Central Monitors</li>\n<li>Ensure quality of clinical monitoring, central monitoring, and site management deliverables</li>\n<li>Review project oversight dashboards and clinical trial systems to ensure data accuracy and timeliness</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent experience</li>\n<li>Demonstrated ability to lead and align teams in achieving project milestones</li>\n<li>Experience working in an international environment</li>\n<li>Expertise in site management and monitoring (clinical or central)</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements</li>\n<li>Strong communication, presentation, and interpersonal skills</li>\n<li>Ability to apply problem-solving techniques to resolve complex issues</li>\n<li>Moderate travel required (approximately 20%)</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/SRB-Remote/Clinical-Trial-Manager-ll--Home-based-Serbia_25110792","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/SRB-Remote/Clinical-Trial-Manager-ll--Home-based-Serbia_25110792","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","clinical trial management","risk management","communication","problem-solving"],"x-skills-preferred":["risk-based monitoring"],"datePosted":"2026-10-28T03:21:14.579Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, clinical trial management, risk management, communication, problem-solving, risk-based monitoring"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_bc508ceb-32f"},"title":"Clinical Trial Manager - Full Service","description":"<p>Syneos Health is seeking a Clinical Trial Manager - Full Service. As a Clinical Trial Manager, you will be responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Oversee site interactions post-activation through site closeout, including patient recruitment, investigator payments, and other related activities.</li>\n<li>Review study scope of work, budget, and protocol content, ensuring the clinical project team is aware of contractual obligations and parameters.</li>\n<li>Employ strategic thinking and problem-solving skills to propose and implement risk mitigations.</li>\n<li>Serve as an escalation point for communications with investigator site staff.</li>\n<li>Collaborate with other functional leaders to coordinate delivery handoffs and meet expected study milestones.</li>\n<li>Develop and maintain clinical study tools and templates, including the Clinical Monitoring Plan.</li>\n<li>Coordinate training for the study team regarding protocol specificities, Case Report Form completion, and Sponsor Standard Operating Procedures.</li>\n<li>Oversee resourcing allocations for CRAs and Central Monitors, site assignments, and study team members&#39; conduct.</li>\n<li>Review project oversight dashboards and other clinical trial systems to ensure data has been updated to reflect timely execution of all operational aspects.</li>\n<li>Understand the monitoring strategy required for the study and participate in the development of the study risk assessment plan.</li>\n<li>Review content and quality of site and central monitoring documentation.</li>\n<li>Interact with clients and other functional departments related to clinical monitoring, central monitoring, and site management activities and deliverables.</li>\n<li>Demonstrate understanding of other functions&#39; roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP, and country regulations.</li>\n<li>Oversee CRAs and Central Monitors assigned to the study and assess study-specific process and training compliance.</li>\n<li>Provide feedback to line managers on staff performance.</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience.</li>\n<li>Demonstrated ability to lead and align teams in the achievement of project milestones.</li>\n<li>Demonstrated capability of working in an international environment.</li>\n<li>Demonstrated expertise in site management and monitoring (clinical or central).</li>\n<li>Preferred experience with risk-based monitoring.</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.</li>\n<li>Strong conflict resolution skills.</li>\n<li>Moderate travel may be required, approximately 20%.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Trial-Manager---Full-Service_25110988","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Trial-Manager---Full-Service_25110988","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"The base salary range represents the anticipated low and high of the Syneos Health range for this position.","x-skills-required":["Good Clinical Practice","ICH Guidelines","Risk-Based Monitoring","Site Management","Clinical Monitoring","Central Monitoring","Protocol Development","Budget Management","Conflict Resolution"],"x-skills-preferred":[],"datePosted":"2026-10-28T03:05:23.855Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, Risk-Based Monitoring, Site Management, Clinical Monitoring, Central Monitoring, Protocol Development, Budget Management, Conflict Resolution"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d648ecaf-31f"},"title":"FSO Experienced CRA","description":"<p>Syneos Health is seeking an experienced Clinical Research Associate (CRA) to join their team. The successful candidate will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits. The CRA will ensure regulatory, ICH-GCP, and protocol compliance, and provide recommendations regarding site-specific actions.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Ensure regulatory, ICH-GCP, and protocol compliance</li>\n<li>Evaluate overall performance of site and site staff and provide recommendations</li>\n<li>Verify process of obtaining informed consent and document confidentiality of subjects/patients</li>\n<li>Assess factors affecting subject/patient safety and clinical data integrity</li>\n<li>Conduct Source Document Review and verify clinical data entered in case report forms</li>\n<li>Apply query resolution techniques and provide guidance to site staff</li>\n<li>Utilize available hardware and software to support clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>Perform 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Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/JPN-Tokyo-Hybrid/FSO-CRA-II---Sr-CRA_25107273","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory compliance","clinical research","site management"],"x-skills-preferred":[],"datePosted":"2026-10-28T03:05:17.926Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory compliance, clinical research, site management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b77a3bb7-688"},"title":"Clinical Research Associate (CRA)","description":"<p>Syneos Health is seeking a Clinical Research Associate (CRA) to join their team in Portugal.</p>\n<p>As a CRA, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating the overall performance of site and site staff and providing recommendations regarding site-specific actions</li>\n<li>Communicating and escalating serious issues to the project team and developing action plans</li>\n<li>Maintaining a working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes</li>\n<li>Verifying the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assessing factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conducting Source Document Review of appropriate site source documents and 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standards</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to adapt to new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/JPN-Osaka/CRA--Future-Roles-_25106960","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos 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leading fully-integrated life sciences services organisation built to accelerate customer success.</p>\n<p>The Clinical Trial Manager will be responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Oversees site interactions post-activation through site closeout</li>\n<li>Identifies critical data and processes, protocol execution risks, and risk mitigations</li>\n<li>Reviews study scope of work, budget, and protocol content</li>\n<li>Uses prior clinical experience, operational data, metrics, and reports to identify risks</li>\n<li>Escalates risks to clinical trial management deliverables to the project manager</li>\n<li>Employs strategic thinking and problem-solving skills to propose and implement risk mitigations</li>\n<li>Participates in key meetings such as Kick Off Meetings</li>\n<li>Serves as an escalation point for communications with investigator site staff</li>\n<li>Collaborates with other functional leaders to coordinate delivery handoffs and meet expected study milestones</li>\n<li>Develops and maintains clinical study tools and templates</li>\n<li>Coordinates training to the study team</li>\n<li>Oversees resourcing allocations for CRAs and Central Monitors</li>\n<li>Ensures quality of clinical monitoring, central monitoring, and site management deliverables</li>\n<li>Reviews project oversight dashboards and other clinical trial systems</li>\n<li>Understands the monitoring strategy required for the study</li>\n<li>Reviews content and quality of site and central monitoring documentation</li>\n<li>Interacts with clients and other functional departments</li>\n<li>Demonstrates understanding of other functions&#39; roles in achieving compliance and delivery</li>\n<li>Oversees CRAs and Central Monitors assigned to the study</li>\n<li>Provides feedback to line managers on staff performance</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Demonstrated ability to lead and align teams in the achievement of project milestones</li>\n<li>Demonstrated capability of working in an international environment</li>\n<li>Demonstrated expertise in site management and monitoring</li>\n<li>Preferred experience with risk-based monitoring</li>\n<li>Demonstrates understanding of clinical trial management financial principles and budget management</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills</li>\n<li>Strong conflict resolution skills</li>\n<li>Demonstrated ability to apply problem-solving techniques to resolve complex issues</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/POL-Remote/Global-Clinical-Trial-Manager-II-or-Senior--Home-based-Poland_25113637","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/POL-Remote/Global-Clinical-Trial-Manager-II-or-Senior--Home-based-Poland_25113637","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","clinical trial management","budget management","conflict resolution","problem-solving"],"x-skills-preferred":["risk-based monitoring"],"datePosted":"2026-10-28T00:17:25.082Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, clinical trial management, budget management, conflict resolution, problem-solving, risk-based monitoring"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_84eb3076-792"},"title":"Clinical Research Coordinator","description":"<p>We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Perform various clinical procedures, including ECG, sample collection, and vital signs.</li>\n<li>Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.</li>\n<li>Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.</li>\n<li>Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.</li>\n<li>Collect and accurately record clinical data in case report forms (CRFs).</li>\n<li>Collaborate with investigators and monitors, addressing queries and ensuring data quality.</li>\n<li>Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree preferred or equivalent combination of education and relevant experience.</li>\n<li>Minimum 1+ years of relevant work experience in clinical research.</li>\n<li>Working knowledge of clinical trials, GCP principles, and medical terminology.</li>\n<li>Strong attention to detail and ability to establish effective working relationships.</li>\n<li>Proficiency with EDC systems, data entry accuracy, and query management.</li>\n</ul>\n<p>The potential base pay range for this role is $35.00-$42.00 per hour.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Jefferson-City-MO/Clinical-Research-Coordinator---Jefferson-City--MO_R1561898","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Jefferson-City-MO/Clinical-Research-Coordinator---Jefferson-City--MO_R1561898","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"part-time","x-salary-range":"$35.00-$42.00 per hour","x-skills-required":["clinical research","Good Clinical Practice","EDC systems","data entry","medical terminology"],"x-skills-preferred":[],"datePosted":"2026-10-28T00:16:09.535Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Jefferson City, MO"}},"employmentType":"PART_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"clinical research, Good Clinical Practice, EDC systems, data entry, medical terminology"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_b3354b4a-324"},"title":"Experienced Clinical Research Associate - Sponsor Dedicated","description":"<p>Syneos Health is seeking an Experienced Clinical Research Associate - Sponsor Dedicated. The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits. They will verify the process of obtaining informed consent, assess factors affecting subject/patient safety and clinical data integrity, and apply query resolution techniques. The CRA will also maintain a working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity</li>\n<li>Apply query resolution techniques remotely and on-site</li>\n<li>Maintain a working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Supports subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enters data into tracking systems as required</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provides guidance at the site and project level towards audit readiness standards</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to embrace new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Company car or car allowance</li>\n<li>Health benefits, including Medical, Dental, and Vision</li>\n<li>Company match 401k</li>\n<li>Eligibility to participate in Employee Stock Purchase Plan</li>\n<li>Eligibility to earn commissions/bonus based on company and individual performance</li>\n<li>Flexible paid time off (PTO) and sick time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Experienced-Clinical-Research-Associate---Sponsor-Dedicated_25109784","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Experienced-Clinical-Research-Associate---Sponsor-Dedicated_25109784","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$base salary range represents the anticipated low and high of the Syneos Health range for this position","x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T00:07:20.366Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_7772b9c5-209"},"title":"Clinical Research Associate","description":"<p>Syneos Health is seeking a Clinical Research Associate. As a Clinical Research Associate, you will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Supports subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enters data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Company car or car allowance</li>\n<li>Health benefits to include Medical, Dental, and Vision</li>\n<li>Company match 401k</li>\n<li>Eligibility to participate in Employee Stock Purchase Plan</li>\n<li>Eligibility to earn commissions/bonus based on company and individual performance</li>\n<li>Flexible paid time off (PTO) and sick time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Research-Associate---Full-Service_25109785","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Research-Associate---Full-Service_25109785","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$base salary range represents the anticipated low and high of the Syneos Health range for this position","x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T00:07:01.068Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_86836d8b-f7f"},"title":"CRA II - Oncology / Ophthalmology","description":"<p>Syneos Health is seeking a CRA II - Oncology / Ophthalmology. The successful candidate will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>Verify site compliance with electronic data capture requirements</li>\n<li>Perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution</li>\n<li>Understand project scope, budgets, and timelines; manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>Act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to embrace new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Company car or car allowance</li>\n<li>Health benefits, including Medical, Dental, and Vision</li>\n<li>Company match 401k</li>\n<li>Eligibility to participate in Employee Stock Purchase Plan</li>\n<li>Eligibility to earn commissions/bonus based on company and individual performance</li>\n<li>Flexible paid time off (PTO) and sick time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-IL-Remote/CRA-II---Oncology---Ophthalmology--Home-Based---Midwestern-Region-_25111405","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-IL-Remote/CRA-II---Oncology---Ophthalmology--Home-Based---Midwestern-Region-_25111405","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$base salary range represents the anticipated low and high of the Syneos Health range for this position","x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-28T00:06:42.746Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_47ce692e-7d8"},"title":"Clinical Trial Manager I - 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This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.</p>\n<p><strong>Key Responsibilities</strong></p>\n<ul>\n<li>Perform accurate EDC data entry, manage queries, and ensure timely resolution.</li>\n<li>Maintain and update the regulatory binder in compliance with documentation and audit standards.</li>\n<li>Coordinate and schedule subject visits, procedures, and follow-up activities.</li>\n<li>Build effective working relationships with investigators, clinical staff, and study team members.</li>\n<li>Support subject screening, recruitment, and enrollment activities.</li>\n<li>Assist with patient/research participant scheduling and collection of medical history.</li>\n<li>Coordinate lab procedures and follow-up care in alignment with study protocols.</li>\n<li>Ensure strict adherence to IRB-approved protocols, including assistance with informed consent processes.</li>\n<li>Uphold participant safety and report concerns promptly per SOPs and Sponsor requirements.</li>\n<li>Follow all company policies, SOPs, guidelines, and Good Clinical Practice (GCP) standards.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Associate degree preferred or equivalent combination of education and relevant experience.</li>\n<li>1+ years of experience in a clinical research environment preferred.</li>\n<li>Strong working knowledge of clinical trials, GCP, and protocol-specific procedures.</li>\n<li>Proficiency with EDC systems, data entry accuracy, and query management.</li>\n<li>Experience with visit scheduling, regulatory documentation, and binder maintenance.</li>\n<li>Excellent attention to detail, time management, and task prioritization.</li>\n<li>Strong communication, interpersonal, and relationship-building skills.</li>\n</ul>\n<p>The potential base pay range for this role is $25.00-$39.00 per hour.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kansas-City-MO/Site-Research-Assistant---Kansas-City--MO_R1561497","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kansas-City-MO/Site-Research-Assistant---Kansas-City--MO_R1561497","x-work-arrangement":"onsite","x-experience-level":null,"x-job-type":null,"x-salary-range":"$25.00-$39.00 per hour","x-skills-required":["EDC systems","data entry","clinical trials","GCP","protocol-specific procedures","regulatory documentation","Good Clinical Practice"],"x-skills-preferred":["associate degree","1+ years of experience in clinical research environment","visit scheduling","binder maintenance","relationship-building skills"],"datePosted":"2026-10-27T23:30:17.233Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Kansas City, MO"}},"occupationalCategory":"Research","industry":"Healthcare","skills":"EDC systems, data entry, clinical trials, GCP, protocol-specific procedures, regulatory documentation, Good Clinical Practice, associate degree, 1+ years of experience in clinical research environment, visit scheduling, binder maintenance, relationship-building skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_967984cd-91d"},"title":"CRA 2","description":"<p>Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes.</li>\n<li>May perform investigational product (IP) inventory, reconciliation and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.</li>\n<li>For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.</li>\n<li>May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate.</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/TWN-Taipei-Hybrid/CRA-2_25113675-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/TWN-Taipei-Hybrid/CRA-2_25113675-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH 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site-specific actions</li>\n<li>Verifying informed consent processes and protecting subject/patient confidentiality</li>\n<li>Assessing site processes and conducting source document reviews</li>\n<li>Applying query resolution techniques and providing guidance to site staff</li>\n<li>Managing investigational product inventory and verifying dispensing and administration</li>\n<li>Reviewing investigator site files and trial master files</li>\n<li>Documenting activities and supporting subject/patient recruitment and retention</li>\n<li>Understanding project scope, budgets, and timelines</li>\n<li>Acting as a primary liaison with project site personnel</li>\n<li>Providing guidance on audit readiness standards</li>\n<li>May provide training or mentorship to junior CRAs</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree or RN in a related field</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75%</li>\n</ul>\n<p>Syneos Health offers a range of benefits, including career development and progression opportunities, technical and therapeutic area training, and a total rewards program.</p>\n<p>The company is committed to building an inclusive culture and has a strong focus on delivering high-quality services to customers.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/TWN-Taipei-Hybrid/Sr-CRA-1_25113673","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/TWN-Taipei-Hybrid/Sr-CRA-1_25113673","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","communication","presentation","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-27T23:22:23.933Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, communication, presentation, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_2b5e3efb-2ab"},"title":"Clinical Research Associate II - Beijing","description":"<p>Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance.</li>\n<li>Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site.</li>\n<li>For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes, Conducts Source Document Review of appropriate site source documents and medical records.</li>\n<li>May perform investigational product (IP) inventory, reconciliation and reviews storage and security.</li>\n<li>Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.</li>\n<li>Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.</li>\n<li>For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met.</li>\n<li>May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA).</li>\n<li>Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.</li>\n<li>Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.</li>\n</ul>\n<p><strong>Qualifications</strong></p>\n<ul>\n<li>Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/CRAI-II-Beijing_25113647","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/CRAI-II-Beijing_25113647","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-27T23:21:52.097Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ace01413-b82"},"title":"Clinical Research Associate","description":"<p>IQVIA Turkey is looking for a talented and motivated team member to join their Sponsor dedicated team as an experienced Clinical Research Associate (CRA).</p>\n<p>In this role, you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within the organization.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Performing site selection, initiation, monitoring and close-out visits</li>\n<li>Supporting the development of a subject recruitment plan</li>\n<li>Evaluating the quality and integrity of site practices in accordance with regulatory requirements, such as Good Clinical Practice and International Conference on Harmonization guidelines</li>\n<li>Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions</li>\n<li>Collaborating with experts at study sites and with client representatives</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>University degree in a scientific discipline or healthcare</li>\n<li>At least 6 months of on-site monitoring experience</li>\n<li>Experience in the Pharma industry and/or Clinical Trials environment</li>\n<li>Very good computer skills, including MS Office</li>\n<li>Excellent command of Turkish and English languages</li>\n<li>Organizational, time management and problem-solving skills</li>\n<li>Ability to establish and maintain effective working relationships with co-workers, managers, and clients</li>\n<li>Flexibility to travel</li>\n<li>Driver’s license class B</li>\n</ul>\n<p><strong>What you can expect:</strong></p>\n<ul>\n<li>Resources that promote your career growth</li>\n<li>Leaders that support flexible work schedules</li>\n<li>Programs to help you build your therapeutic knowledge</li>\n<li>Excellent working environment in a stable, international, reputable company</li>\n<li>Company car, mobile phone and attractive benefits package</li>\n</ul>\n<p>For candidates able to start before September 2026, a discretionary sign-on bonus of up to 210,000 TRY may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Istanbul-Turkey/Experienced-Clinical-Research-Associate---Sponsor-dedicated---Trkiye_R1537437","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Turkey","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Istanbul-Turkey/Experienced-Clinical-Research-Associate---Sponsor-dedicated---Trkiye_R1537437","x-work-arrangement":"onsite","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["MS 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The successful candidate will perform site qualification, site initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on-site, and provide 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submitting regular visit reports, generating follow-up letters and other required study documentation</li>\n<li>Collaborate and liaise with study team members for project execution support as appropriate</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s and Master&#39;s Degree in scientific discipline or health care</li>\n<li>At least 3 years of on-site monitoring experience</li>\n<li>CRA Certification according to Ministerial Decree dated 15.11.2011</li>\n<li>Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (GCP and ICH guidelines)</li>\n<li>Good therapeutic and protocol knowledge as provided in company training</li>\n<li>Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable)</li>\n<li>Written and verbal communication skills including good command of English language</li>\n<li>Organizational and problem-solving 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Key responsibilities include:</p>\n<ul>\n<li>Managing the overall operational aspects of clinical trial projects, from study initiation through to close-out.</li>\n<li>Collaborating with cross-functional teams to develop study plans, timelines, and budgets, ensuring alignment with project goals.</li>\n<li>Overseeing the performance of Clinical Trial Managers and study teams, providing guidance and support as needed.</li>\n<li>Ensuring compliance with regulatory requirements, Good Clinical Practice (GCP), and internal policies throughout the trial process.</li>\n<li>Identifying risks and implementing strategies to mitigate them, ensuring the successful delivery of clinical trials.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. 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The successful candidate will be responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Overseeing site interactions post-activation through site closeout</li>\n<li>Identifying critical data and processes, protocol execution risks, and risk mitigations</li>\n<li>Reviewing study scope of work, budget, and protocol content</li>\n<li>Using prior clinical experience, operational data, metrics, and reports to identify risks to clinical trial management deliverables</li>\n<li>Escalating risks to clinical trial management deliverables to the project manager</li>\n<li>Employing strategic thinking and problem-solving skills to propose and implement risk mitigations</li>\n<li>Participating in key meetings such as Kick Off Meetings</li>\n<li>Serving as an escalation point for communications with investigator site 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performance</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Demonstrated ability to lead and align teams in the achievement of project milestones</li>\n<li>Demonstrated capability of working in an international environment</li>\n<li>Demonstrated expertise in site management and monitoring</li>\n<li>Preferred experience with risk-based monitoring</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills</li>\n<li>Good communication, presentation, and interpersonal skills</li>\n<li>Strong conflict resolution skills</li>\n<li>Moderate travel may be required, approximately 20%</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GRC-Athens-Hybrid/Clinical-Trial-Manager-II_25113657","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GRC-Athens-Hybrid/Clinical-Trial-Manager-II_25113657","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","clinical trial management","site management","monitoring","risk-based monitoring","budget management","conflict resolution","problem-solving"],"x-skills-preferred":[],"datePosted":"2026-10-27T22:41:59.807Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good 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escalate serious issues to the project team and develop action plans</li>\n<li>Maintain a working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on-site, and provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support the effective conduct of the clinical study data review and capture</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and 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communication, presentation, and interpersonal skills.</li>\n<li>Ability to manage required travel of up to 75% on a regular basis.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Client/CRA-II-based-in-Korea_25113839","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Client/CRA-II-based-in-Korea_25113839","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal 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benefits, including career development and progression, supportive line management, technical and therapeutic area training, and a total rewards program.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/PMII_25113786","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/PMII_25113786","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH guidelines","project management","clinical research","regulatory requirements"],"x-skills-preferred":["clinical research organization (CRO)","therapeutic 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schedules</li>\n<li>Programs to help you build your therapeutic knowledge</li>\n<li>An excellent working environment in a stable, international, reputable company</li>\n<li>A company car, mobile phone, and attractive benefits package</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Lisbon-Portugal/Clinical-Research-Associate-2---Based-in-Portugal_R1513619","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Lisbon-Portugal/Clinical-Research-Associate-2---Based-in-Portugal_R1513619","x-work-arrangement":null,"x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["MS Office","Portuguese","English","Good Clinical 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Sydney-North-New-South-Wales-Australia/Senior---Clinical-Research-Associate_R1525252","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Sydney-North-New-South-Wales-Australia/Senior---Clinical-Research-Associate_R1525252","x-work-arrangement":null,"x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","International Conference on Harmonization guidelines","Microsoft Word","Excel","PowerPoint","English"],"x-skills-preferred":[],"datePosted":"2026-10-27T22:28:06.381Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, International Conference on Harmonization guidelines, 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skills.</li>\n<li>Ability to manage required travel of up to 75% on a regular basis.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/Senior-CRA-Germany_25113690","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/Senior-CRA-Germany_25113690","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","German","English","Clinical 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environment where you can develop your skills and advance your career.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Remote/Sr-CRA---FSP---Homebased-across-Romania_25113905","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ROU-Remote/Sr-CRA---FSP---Homebased-across-Romania_25113905","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal 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maintain effective working relationships with coworkers, managers, and clients.</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Hong-Kong/CRA-HK_R1528418","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Hong-Kong/CRA-HK_R1528418","x-work-arrangement":null,"x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","International Conference on Harmonization","Microsoft Word","Excel","PowerPoint","English"],"x-skills-preferred":[],"datePosted":"2026-10-27T22:12:47.391Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, International 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The Clinical Trial Manager will be responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Responsible for site management oversight, clinical monitoring, and central monitoring deliverables</li>\n<li>Oversees site interactions post-activation through site closeout</li>\n<li>May be responsible for identification of critical data and process, protocol execution risks, and risk mitigations</li>\n<li>Reviews the study scope of work, budget, and protocol content</li>\n<li>Uses prior clinical experience, operational data, metrics, and reports to identify risks to clinical trial management deliverables</li>\n<li>Escalates to the project manager any risks to clinical trial management deliverables</li>\n<li>Employs strategic thinking and problem-solving skills to propose and implement risk mitigations</li>\n<li>Participates and presents in key meetings</li>\n<li>Serves as an escalation point for communications with investigator site staff</li>\n<li>Collaborates with other functional leaders to coordinate delivery handoffs and meet expected study milestones</li>\n<li>Responsible for development and ongoing maintenance of clinical study tools and templates</li>\n<li>Coordinates initial and ongoing training to the study team</li>\n<li>Oversees resourcing allocations for CRAs and Central Monitors, site assignments, and study team members&#39; conduct</li>\n<li>Ensures quality of the clinical monitoring, central monitoring, and site management deliverables</li>\n<li>Reviews the project oversight dashboards and other clinical trial systems</li>\n<li>Understands the monitoring strategy required for the study and participates in the development of the study risk assessment plan</li>\n<li>Reviews the content and quality of site and central monitoring documentation</li>\n<li>Interacts with the client and other functional departments related to clinical monitoring, central monitoring, and site management activities and deliverables</li>\n<li>Demonstrates understanding of other functions&#39; roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP, and country regulations</li>\n<li>Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance</li>\n<li>Provides feedback to line managers on staff performance</li>\n</ul>\n<p><strong>Qualifications:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Demonstrated ability to lead and align teams in the achievement of project milestones</li>\n<li>Demonstrated capability of working in an international environment</li>\n<li>Demonstrated expertise in site management and monitoring (clinical or central)</li>\n<li>Preferred experience with risk-based monitoring</li>\n<li>Demonstrates understanding of clinical trial management financial principles and budget management</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Must demonstrate good computer skills</li>\n<li>Good communication, presentation, and interpersonal skills among project team and with sites</li>\n<li>Strong conflict resolution skills</li>\n<li>Demonstrated ability to apply problem-solving techniques to resolve complex issues</li>\n<li>Critical thinking to determine the cause and appropriate solution in the identification of issues</li>\n<li>Moderate travel may be required, approximately 20%</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CAN-Remote/Clinical-Trial-Manager_25107759","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CAN-Remote/Clinical-Trial-Manager_25107759","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","clinical trial management","budget management","risk-based monitoring","conflict resolution","problem-solving"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:45:28.107Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, clinical trial management, budget management, risk-based monitoring, conflict resolution, problem-solving"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_dccaaaa6-7b8"},"title":"Sr. CRA 1","description":"<p>IQVIA Biotech is seeking a Senior Clinical Research Associate (CRA) to work in Brazil, preferably with oncology experience.</p>\n<p>As a Sr. CRA, you will perform monitoring and site management work to ensure that sites are conducting studies and reporting study data according to the study protocol, regulations, guidelines, and sponsor requirements.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Conducting site monitoring visits (selection, initiation, monitoring, and close-out) in accordance with the contracted scope of work and Good Clinical Practice</li>\n<li>Working with sites to adapt, drive, and track subject recruitment plans to enhance predictability</li>\n<li>Providing protocol and study-related training to assigned sites and establishing regular communication channels</li>\n<li>Evaluating the quality and integrity of study site practices and escalating quality issues as needed</li>\n<li>Managing study progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolution</li>\n<li>Ensuring site documents are available for filing in the Trial Master File (TMF) and verifying that the Investigator&#39;s Site File (ISF) is maintained according to GCP and local regulations</li>\n<li>Creating and maintaining documentation regarding site management, monitoring visit findings, and action plans</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific discipline or healthcare (preferred)</li>\n<li>At least 3-4 years of on-site monitoring experience</li>\n<li>Equivalent combinations of education, training, and experience may be considered</li>\n<li>Good knowledge of and skill in applying applicable clinical research regulatory requirements</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-CRA-1--Brazil_R1543982","directApply":true,"hiringOrganization":{"@type":"Organization","name":"IQVIA Biotech","sameAs":"https://jobs.iqvia.com","logo":"https://logos.yubhub.co/jobs.iqvia.com.png"},"x-apply-url":"https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-CRA-1--Brazil_R1543982","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","clinical research regulatory requirements","site management","monitoring"],"x-skills-preferred":["oncology"],"datePosted":"2026-10-27T21:44:23.863Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, clinical research regulatory requirements, site management, monitoring, oncology"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_39537fbb-2d6"},"title":"Clinical Research Associate I","description":"<p>Syneos Health is seeking a Clinical Research Associate I to perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits. The successful candidate will have a Bachelor&#39;s degree or RN in a related field, knowledge of Good Clinical Practice/ICH Guidelines, and excellent communication and interpersonal skills.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff, and provide recommendations regarding site-specific actions</li>\n<li>Verify process of obtaining informed consent, assess factors affecting subject/patient safety and clinical data integrity</li>\n<li>Conduct Source Document Review, verify required clinical data entered in case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques, provide guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support clinical project data review and capture</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at site and project level towards audit readiness standards</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to adapt to new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p>Benefits:</p>\n<ul>\n<li>Company car or car allowance</li>\n<li>Health benefits, including Medical, Dental, and Vision</li>\n<li>Company match 401k</li>\n<li>Eligibility to participate in Employee Stock Purchase Plan</li>\n<li>Eligibility to earn commissions/bonus based on company and individual performance</li>\n<li>Flexible paid time off (PTO) and sick time</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Morrisville-Hybrid/CTM---Future-Roles--US-_25107098","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Morrisville-Hybrid/CTM---Future-Roles--US-_25107098","x-work-arrangement":"hybrid","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":"$base salary range represents the anticipated low and high of the Syneos Health range for this position","x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:34:12.427Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_9c4d13e0-90e"},"title":"Clinical Research Associate (CRA)","description":"<p>Syneos Health is seeking a Clinical Research Associate (CRA) to join their team. The CRA will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions</li>\n<li>Verify process of obtaining informed consent and document confidentiality of each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity</li>\n<li>Conduct Source Document Review and verify required clinical data entered in case report form (CRF)</li>\n<li>Apply query resolution techniques and provide guidance to site staff</li>\n<li>Utilize available hardware and software to support clinical project data review and capture</li>\n<li>Perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required</li>\n<li>Prepare for and attend Investigator Meetings and sponsor face-to-face meetings</li>\n<li>Provide guidance at site and project level towards audit readiness standards</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to adapt to new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CAN-ON-Toronto-Hybrid/CRA---Future-roles--Canada-_25107094","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CAN-ON-Toronto-Hybrid/CRA---Future-roles--Canada-_25107094","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:31:22.027Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_6d883f4a-48c"},"title":"Clinical Research Associate","description":"<p>Syneos Health is seeking a Clinical Research Associate to join their team.</p>\n<p>The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating site performance and providing recommendations for site-specific actions</li>\n<li>Verifying informed consent and protecting subject/patient confidentiality</li>\n<li>Assessing site processes and conducting source document reviews</li>\n<li>Applying query resolution techniques and providing guidance to site staff</li>\n<li>Managing investigational product inventory and verifying dispensing and administration</li>\n<li>Reviewing investigator site files and reconciling contents with trial master files</li>\n<li>Documenting activities and supporting subject/patient recruitment and retention</li>\n<li>Preparing for and attending investigator meetings and sponsor face-to-face meetings</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree or RN in a related field or equivalent experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ESP-Madrid-Hybrid/CTM---Future-Roles_25106988","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/ESP-Madrid-Hybrid/CTM---Future-Roles_25106988","x-work-arrangement":"hybrid","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory compliance","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:31:18.245Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory compliance, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_7682855b-616"},"title":"Clinical Research Associate","description":"<p>Syneos Health is seeking a Clinical Research Associate to join their team in Bulgaria.</p>\n<p>The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating site performance and providing recommendations for site-specific actions</li>\n<li>Verifying informed consent and protecting patient confidentiality</li>\n<li>Assessing site processes and conducting source document reviews</li>\n<li>Resolving queries and providing guidance to site staff</li>\n<li>Managing investigational product inventory and verifying dispensing and administration</li>\n<li>Reviewing investigator site files and trial master files</li>\n<li>Documenting activities and supporting subject recruitment and retention</li>\n<li>Collaborating with project teams and site personnel</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to manage required travel of up to 75%</li>\n</ul>\n<p>Syneos Health offers a dynamic work environment, opportunities for career development, and a Total Self culture that encourages authenticity and well-being.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/BGR-Remote/CTM---Future-roles--Bulgaria-_25106971","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos 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Research Associate (CRA) to join their team in Bulgaria.</p>\n<p>As a CRA, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating the overall performance of site and site staff, and providing recommendations regarding site-specific actions</li>\n<li>Verifying the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assessing factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conducting Source Document Review of appropriate site source documents and medical records</li>\n<li>Verifying required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Applying query resolution techniques remotely and on site, and 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Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:31:13.618Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ad28a9b7-94f"},"title":"Clinical Research Associate (CRA)","description":"<p>Syneos Health is seeking a Clinical Research Associate (CRA) to join their team in Turkey.</p>\n<p>As a CRA, you will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating the overall performance of site and site staff and providing recommendations regarding site-specific actions</li>\n<li>Communicating and escalating serious issues to the project team and developing action plans</li>\n<li>Maintaining a working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes</li>\n<li>Verifying the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assessing factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conducting Source Document Review of appropriate site source documents and medical records</li>\n<li>Applying query resolution techniques remotely and on-site, and providing guidance to site staff as necessary</li>\n<li>Managing site-level activities and communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>Preparing for and attending Investigator Meetings and/or 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priorities to achieve goals/targets</li>\n<li>Act as primary liaison with project site personnel or in collaboration with Central Monitoring Associate</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions</li>\n<li>May provide training or mentorship to more junior level CRAs</li>\n<li>May perform training and sign-off visits for junior CRA staff, as assigned</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Good computer skills and ability to adapt to new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Basic level of critical thinking skills expected</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Remote/Sr-CRA-I---Shenyang_25113631","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Remote/Sr-CRA-I---Shenyang_25113631","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills","critical thinking"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:28:31.100Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills, interpersonal skills, critical thinking"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_7e0c9ec4-333"},"title":"Clinical Research Associate","description":"<p>Syneos Health is seeking an experienced Clinical Research Associate (CRA) to join their team in Germany.</p>\n<p>The successful candidate will perform site qualification, site initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating site performance and providing recommendations for site-specific actions</li>\n<li>Verifying informed consent and protecting subject/patient confidentiality</li>\n<li>Assessing site processes and conducting source document reviews</li>\n<li>Applying query resolution techniques and providing guidance to site staff</li>\n<li>Managing investigational product inventory and verifying dispensing and administration</li>\n<li>Reviewing investigator site files and reconciling contents with trial master files</li>\n<li>Documenting activities and supporting subject/patient recruitment and retention</li>\n<li>Understanding project scope, budgets, and timelines to ensure objectives are met</li>\n<li>Acting as a liaison with project site personnel and providing guidance on audit readiness</li>\n<li>May provide training or mentorship to junior CRAs</li>\n</ul>\n<p>The ideal candidate will have:</p>\n<ul>\n<li>A Bachelor&#39;s degree or RN in a related field or equivalent experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements</li>\n<li>Previous monitoring experience in 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As a Senior CRA, you will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits</li>\n<li>Evaluate overall performance of site and site staff, and provide recommendations regarding site-specific actions</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary</li>\n<li>May perform investigational product (IP) inventory, reconciliation, and reviews storage and security</li>\n<li>Routinely review the Investigator Site File (ISF) for accuracy, timeliness, and completeness</li>\n<li>Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</li>\n<li>Enter data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution</li>\n<li>Understand project scope, budgets, and timelines, and manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate</li>\n<li>Prepare for and attend Investigator Meetings and/or sponsor face-to-face meetings</li>\n<li>Provide guidance at the site and project level towards audit readiness standards and support preparation for audit and required follow-up actions</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree or RN in a related field or equivalent combination of education, training, and experience</li>\n<li>Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements</li>\n<li>Several years of monitoring experience</li>\n<li>Must demonstrate good computer skills and be able to embrace new technologies</li>\n<li>Excellent communication, presentation, and interpersonal skills</li>\n<li>Fluency in German and English</li>\n<li>Location in north Germany, travel in the DACH region may be required</li>\n<li>Ability to manage required travel of up to 75% on a regular basis</li>\n</ul>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">Job Data by <a href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/CRA-II-Germany---multisponsor_25109269","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/DEU-Remote/CRA-II-Germany---multisponsor_25109269","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","monitoring experience","computer skills","German","English"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:27:34.677Z","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, monitoring experience, computer skills, German, English"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_5d08db6f-aa5"},"title":"Clinical Research Associate II","description":"<p>Syneos Health is seeking a Clinical Research Associate II to join their Clinical Solutions team. 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As a Sr CRA, you will be responsible for performing regulatory activities, site qualification, site initiation, interim monitoring, site management, and close-out visits.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance</li>\n<li>Evaluate overall performance of site and site staff, and provide recommendations regarding site-specific actions</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site</li>\n<li>Conduct Source Document Review of appropriate site source documents and medical records</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete</li>\n<li>Apply query resolution techniques 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/HUN-Budapest/Sr-CRA-in-Oncology---Sponsor-dedicated---Home-Based-Hungary_25113219","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/HUN-Budapest/Sr-CRA-in-Oncology---Sponsor-dedicated---Home-Based-Hungary_25113219","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory compliance","clinical research","site management"],"x-skills-preferred":[],"datePosted":"2026-10-27T21:25:10.570Z","jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory compliance, clinical research, site management"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_4163bc26-1be"},"title":"Clinical Research Associate (CRA) Oncology Germany","description":"<p>Syneos Health is seeking an experienced Clinical Research Associate (CRA) for a single-sponsor partnership in Germany.</p>\n<p>The successful candidate will perform site qualification, site initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Evaluating site performance and providing recommendations for site-specific actions</li>\n<li>Verifying 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