<div><h3>Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London</h3><p><b>Updated:</b> Today</p><p><b>Location:</b> London, POST-LON, United Kingdom</p><p><b>Job ID:</b>25109548</p><p><b>Job Responsibilities</b></p><ul><li>Prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions.</li><li>Participate in and manage project meetings and conference calls with CROs, vendors, and multi-functional teams.</li><li>Anticipate obstacles and proactively develop solutions to achieve project goals.</li><li>Develop a general understanding of functional issues and routine project goals from an organizational perspective.</li><li>Participate in abstract presentations, oral presentations, and manuscript development activities.</li><li>Interact and cooperate with individuals in other functional areas to address routine study issues and develop tools and processes that increase measured efficiencies of the project.</li><li>Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).</li><li>Assist in selecting Contract Research Organizations (CROs) or vendors.</li><li>Coordinate CROs and vendors.</li><li>Update study timelines.</li><li>Participate in departmental, or interdepartmental, strategic initiatives under general supervision.</li><li>Review routine data and prepare safety, interim, and final study reports and resolve data discrepancies.</li><li>Conduct site evaluation, initiation, co-monitoring, and closeout visits, in addition to routine monitoring visits.</li><li>Assure site compliance with the protocol and regulatory requirements for assigned studies.</li><li>Draft and coordinate review of protocols, informed consents, case report forms, and study plans as needed.</li></ul><p><b>Skills and Experience</b></p><ul><li>Excellent verbal, written, interpersonal and presentation skills.</li><li>Knowledge of FDA and/or EMA Regulations (or relevant local regulations), ICH Guidelines, and GCP governing the conduct of clinical studies.</li><li>Working knowledge and experience with Word, PowerPoint, Project and Excel.</li><li>At least 4+ years of clinical experience and a BS/BA in a relevant scientific discipline.</li></ul><p><b>EEO Statement</b></p><p>Syneos Health is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.</p></div>