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The CRA II will work closely with the project team 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>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</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/CHN-Client/CRA-II--Shanghai_25114155","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--Shanghai_25114155","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"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory requirements, computer skills, communication skills"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_330577f2-f3c"},"title":"CRA II","description":"<p>Syneos Health is seeking a CRA II to join their Clinical Solutions team. 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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/CRA2_25114209-1","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/CHN-Client/CRA2_25114209-1","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 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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/CHN-Client/CRA-I---Shanghai_25112517","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-I---Shanghai_25112517","x-work-arrangement":null,"x-experience-level":null,"x-job-type":null,"x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T02:23:42.826Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"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_8113ba10-d94"},"title":"CRA II","description":"<p>Syneos Health is seeking a CRA II to join their Clinical Solutions team. As a CRA II, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies</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 defined components of projects or processes within the area of responsibility</li>\n<li>Ensure accurate and timely documentation of monitoring activities and findings</li>\n<li>Collaborate with cross-functional teams to support clinical trial operations</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field or equivalent experience</li>\n<li>Minimum of 2-4 years of experience in clinical research monitoring</li>\n<li>Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and manage multiple priorities</li>\n<li>Proficiency in using clinical trial management systems and other relevant software</li>\n</ul>\n<p>Certifications:</p>\n<ul>\n<li>Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li>\n</ul>\n<p>Necessary Skills:</p>\n<ul>\n<li>Attention to detail and strong analytical skills</li>\n<li>Problem-solving abilities and critical thinking</li>\n<li>Ability to work effectively in a team environment</li>\n<li>Strong organizational and time management skills</li>\n<li>Proficiency in Microsoft Office Suite</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_25112853","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_25112853","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","clinical research monitoring","clinical trial management systems","Microsoft Office Suite","analytical skills","problem-solving abilities","time management skills"],"x-skills-preferred":["Certified Clinical Research Associate (CCRA)"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T01:53:00.956Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical research monitoring, clinical trial management systems, Microsoft Office Suite, analytical skills, problem-solving abilities, time management skills, Certified Clinical Research Associate (CCRA)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_06d24ac6-824"},"title":"CRA I","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 site processes and 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>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/CRA-I---Shanghai_25112543","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-I---Shanghai_25112543","x-work-arrangement":null,"x-experience-level":null,"x-job-type":null,"x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal skills"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-30T01:26:24.936Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"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_9c379c3a-f16"},"title":"CRA II","description":"<p>Syneos Health, a leading life sciences services organization, is seeking a CRA II to join their Clinical Solutions team in Beijing.</p>\n<p>The successful candidate will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices. 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHN-Client/Sr-Site-Activation-Specialist_25112501","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/Sr-Site-Activation-Specialist_25112501","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trials","regulatory affairs","site activation","project 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As a CRA II, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies</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 defined components of projects or processes within the area of responsibility</li>\n<li>Ensure accurate and timely documentation of monitoring activities and findings</li>\n<li>Collaborate with cross-functional teams to support clinical trial operations</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field or equivalent experience</li>\n<li>Minimum of 2-4 years of experience in clinical research monitoring</li>\n<li>Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and manage multiple priorities</li>\n<li>Proficiency in using clinical trial management systems and other relevant software</li>\n</ul>\n<p>Certifications:</p>\n<ul>\n<li>Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li>\n</ul>\n<p>Necessary Skills:</p>\n<ul>\n<li>Attention to detail and strong analytical skills</li>\n<li>Problem-solving abilities and critical thinking</li>\n<li>Ability to work effectively in a team environment</li>\n<li>Strong organizational and time management skills</li>\n<li>Proficiency in Microsoft Office Suite</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-I-II---Shanghai_25000288-1","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/CHN-Client/CRA-I-II---Shanghai_25000288-1","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","clinical research monitoring","clinical trial management systems","Microsoft Office Suite"],"x-skills-preferred":["Certified Clinical Research Associate (CCRA)"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-28T05:46:24.342Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical research monitoring, clinical trial management systems, Microsoft Office Suite, Certified Clinical Research Associate (CCRA)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8484f04b-00e"},"title":"CRA I/II","description":"<p>Syneos Health is seeking a CRA I/II to join their team in Shanghai, Beijing, Guangzhou, or Wuhan.</p>\n<p>As a CRA I/II, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices. You will review study protocols, informed consent forms, and case report forms, and develop and implement tools, procedures, and processes to ensure quality monitoring.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies</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 defined components of projects or processes within the area of responsibility</li>\n<li>Ensure accurate and timely documentation of monitoring activities and findings</li>\n<li>Collaborate with cross-functional teams to support clinical trial operations</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field or equivalent experience</li>\n<li>Minimum of 2-4 years of experience in clinical research monitoring</li>\n<li>Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and manage multiple priorities</li>\n<li>Proficiency in using clinical trial management systems and other relevant software</li>\n</ul>\n<p>Certifications:</p>\n<ul>\n<li>Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li>\n</ul>\n<p>Necessary Skills:</p>\n<ul>\n<li>Attention to detail and strong analytical skills</li>\n<li>Problem-solving abilities and critical thinking</li>\n<li>Ability to work effectively in a team environment</li>\n<li>Strong organizational and time management skills</li>\n<li>Proficiency in Microsoft Office Suite</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-I-II---Shanghai-Beijing-Guangzhou-Wuhan_25000450","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-I-II---Shanghai-Beijing-Guangzhou-Wuhan_25000450","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","clinical research monitoring","clinical trial management systems","Microsoft Office Suite"],"x-skills-preferred":["Certified Clinical Research Associate (CCRA)"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-28T05:46:20.623Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical research monitoring, clinical trial management systems, Microsoft Office Suite, Certified Clinical Research Associate (CCRA)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d7cbedbb-9a1"},"title":"Medical Scientist","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>Our 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 we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.</p>\n<p>We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.</p>\n<p><strong>Job Responsibilities</strong> Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities.</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/medical-scientist_25111969","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/medical-scientist_25111969","x-work-arrangement":null,"x-experience-level":null,"x-job-type":null,"x-salary-range":null,"x-skills-required":[],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-28T04:12:37.097Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"occupationalCategory":"Healthcare","industry":"Healthcare"},{"@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":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-15T00:00:00.000Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"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_7824faa0-e15"},"title":"Project Manager","description":"<p>Syneos Health is seeking a Project Manager to oversee interdisciplinary clinical research studies and ensure compliance with GCP, relevant SOP&#39;s, and regulatory requirements.</p>\n<p>The successful candidate will 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.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Managing projects and ensuring quality, timelines, and budget management</li>\n<li>Coordinating activities and deliverables of all study conduct partners</li>\n<li>Identifying and managing issues proactively</li>\n<li>Ensuring studies are conducted in compliance with GCP, relevant SOP&#39;s, and regulatory 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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 area expertise","new 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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 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, providing 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technologies</li>\n<li>Minimal travel up to 25% may be required</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 has worked with 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products, and has conducted over 200 studies across 73,000 sites and 675,000+ trial patients.</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/Clinical-operations-specialist_25103921","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos 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The ideal candidate will have experience in managing clinical trial supplies, excellent communication and project management skills, and the ability to work in a fast-paced environment.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Manage clinical trial supplies, including forecasting, procurement, and inventory management</li>\n<li>Coordinate with cross-functional teams, including clinical operations, logistics, and quality assurance</li>\n<li>Ensure compliance with regulatory requirements and company policies</li>\n<li>Analyze data and develop reports to support supply chain optimization</li>\n<li>Collaborate with vendors and suppliers to resolve issues and improve performance</li>\n</ul>\n<p>Syneos Health offers a range of benefits, including career development and progression opportunities, supportive and engaged line management, technical and therapeutic area training, peer recognition, and 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/CHN-Client/Clinical-Trial-Supplies-Manager_25102871","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/Clinical-Trial-Supplies-Manager_25102871","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["clinical trial supplies management","project management","regulatory compliance","data analysis","communication"],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T20:12:15.638Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Logistics & Supply Chain","industry":"Healthcare","skills":"clinical trial supplies management, project management, regulatory compliance, data analysis, communication"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8dcb20b5-3fe"},"title":"Clinical Research Associate I","description":"<p>Syneos Health is seeking a Clinical Research Associate I to join their team. 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, 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 site source documents and medical records</li>\n<li>Apply query resolution techniques remotely and on-site, providing guidance to site staff as necessary</li>\n<li>Utilize available hardware and software to support effective conduct of 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 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>Understand project scope, budgets, and timelines for own and others&#39; activities in the clinical team</li>\n<li>Manage site-level activities/communication to ensure project objectives, deliverables, and timelines are met</li>\n<li>Adapt to changing 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</li>\n<li>May provide training or mentorship to more junior level CRAs</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/CHN-Client/SCRA-I_25102823","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/SCRA-I_25102823","x-work-arrangement":null,"x-experience-level":"entry","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":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T20:12:14.197Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"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_a01fb227-73d"},"title":"CRA II-Shanghai","description":"<p>Syneos Health is seeking a CRA II to work in Shanghai. 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As a Sr CRA I, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Conduct on-site and remote monitoring of clinical research studies</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 defined components of projects or processes within the area of responsibility</li>\n<li>Ensure accurate and timely documentation of monitoring activities and findings</li>\n<li>Collaborate with cross-functional teams to support clinical trial operations</li>\n</ul>\n<p>Qualifications:</p>\n<ul>\n<li>Bachelor&#39;s degree in a related field or equivalent experience</li>\n<li>Minimum of 2-4 years of experience in clinical research monitoring</li>\n<li>Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements</li>\n<li>Excellent communication and interpersonal skills</li>\n<li>Ability to work independently and manage multiple priorities</li>\n<li>Proficiency in using clinical trial management systems and other relevant software</li>\n</ul>\n<p>Certifications:</p>\n<ul>\n<li>Certified Clinical Research Associate (CCRA) or equivalent certification preferred</li>\n</ul>\n<p>Necessary Skills:</p>\n<ul>\n<li>Attention to detail and strong analytical skills</li>\n<li>Problem-solving abilities and critical thinking</li>\n<li>Ability to work effectively in a team environment</li>\n<li>Strong organizational and time management skills</li>\n<li>Proficiency in Microsoft Office Suite</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_25000388","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_25000388","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice (GCP)","clinical research monitoring","clinical trial management systems","Microsoft Office Suite"],"x-skills-preferred":["Certified Clinical Research Associate (CCRA)"],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T09:46:03.746Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice (GCP), clinical research monitoring, clinical trial management systems, Microsoft Office Suite, Certified Clinical Research Associate (CCRA)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_ebd510b7-058"},"title":"Employee Wellness Specialist","description":"<p>Syneos Health is seeking an Employee Wellness Specialist in Dalian.</p>\n<p>As an Employee Wellness Specialist, you will play a crucial role in promoting employee well-being and supporting a healthy work environment.</p>\n<p><strong>Job Responsibilities</strong></p>\n<ul>\n<li>Develop and implement employee wellness programs to promote physical and mental well-being</li>\n<li>Collaborate with cross-functional teams to create a supportive work environment</li>\n<li>Analyze employee feedback and data to identify areas for improvement</li>\n<li>Design and deliver wellness initiatives and events</li>\n<li>Provide resources and support to employees to manage stress and improve work-life balance</li>\n</ul>\n<p><strong>About Syneos Health</strong></p>\n<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>What We Offer</strong></p>\n<ul>\n<li>Career development and progression opportunities</li>\n<li>Supportive and engaged line management</li>\n<li>Technical and therapeutic area training</li>\n<li>Peer recognition and total rewards program</li>\n<li>Inclusive culture where you can authentically be yourself</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/Employee-Wellness-Specialist_25108268","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/Employee-Wellness-Specialist_25108268","x-work-arrangement":null,"x-experience-level":null,"x-job-type":null,"x-salary-range":null,"x-skills-required":[],"x-skills-preferred":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-27T09:44:51.132Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"occupationalCategory":"Human Resources","industry":"Healthcare"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_3e047d94-e7a"},"title":"CRA I","description":"<p>Syneos Health is seeking a CRA I to join their Clinical Solutions team in Shanghai.</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 ensuring compliance with regulations</li>\n<li>Documenting activities and supporting subject/patient recruitment and retention</li>\n<li>Collaborating with study site personnel and central monitoring associates</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/CHN-Client/CRA-I---Shanghai_25112514","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-I---Shanghai_25112514","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":[],"x-benefits":[],"x-licences":[],"x-visa-sponsorship":"unknown","x-visa-sponsorship-text":null,"x-work-authorisation":"unknown","x-work-authorisation-text":null,"datePosted":"2026-10-26T15:30:07.577Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CHN-Client"}},"employmentType":"FULL_TIME","occupationalCategory":"Healthcare","industry":"Healthcare","skills":"Good Clinical Practice, ICH Guidelines, regulatory compliance, communication skills, interpersonal skills"}]}