{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/mex-client/"},"x-facet":{"type":"city","slug":"mex-client","display":"Mex-client","count":3},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_bc682ecd-43a"},"title":"CTM II","description":"<p>Syneos Health is seeking a CTM II to join their Clinical Solutions team. 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>Responsibilities:</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>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>Demonstrates 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budget management, risk-based monitoring, conflict resolution, problem-solving"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_a7c7c22e-753"},"title":"Site Activation Manager","description":"<p>Syneos Health is seeking a Site Activation Manager to lead and manage Site Start-Up (SSU) deliverables within a country, region or globally, within assigned projects or programs.</p>\n<p>The successful candidate will be responsible and accountable for the customer-focused leadership and management of SSU deliverables, ensuring delivery of activation-ready study sites on time, on budget, and in compliance with all applicable regulations.</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Developing and managing integrated site start-up timelines and reporting progress</li>\n<li>Providing oversight of all project start-up deliverables, including site selection, site activation, and life cycle maintenance</li>\n<li>Collaborating with major functional areas, including Business Development, Alliance Management, and Project Management</li>\n<li>Identifying and evaluating fundamental issues pertaining to Site Start-Up and implementing solutions</li>\n<li>Ensuring all project deliverables meet internal and customer expectations</li>\n<li>Developing and maintaining relationships with customers</li>\n<li>Preparing and presenting overall SSU strategy and status at client meetings</li>\n<li>Reviewing project SSU budget and taking corrective measures to ensure project profitability</li>\n<li>Using professionally recognized tools for planning and management of scope, timeline, and resources</li>\n</ul>\n<p>The ideal candidate will have experience in site activation, project management, and regulatory affairs, with excellent communication and leadership skills.</p>\n<p>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/MEX-Client/Site-Activation-Manager-assigned-to-Client_25109692","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/MEX-Client/Site-Activation-Manager-assigned-to-Client_25109692","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["site activation","project management","regulatory 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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</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity</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</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, and other required project documents</li>\n<li>Support subject/patient recruitment, retention, and awareness strategies</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>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/MEX-Client/Sr-CRA_25105592","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos 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