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Director, Clinical Safety at Jobgether. This position is posted by Jobgether on behalf of MCRA. We are currently looking for a . Director, Clinical Safety. in . District of Columbia (USA).. As a Director of Clinical Safety, you will play a critical leadership role in overseeing safety-related operations across multiple clinical trials. This position requires in-depth collaboration with cross-functional teams to ensure high-quality execution of safety reviews, CEC and DSMB processes, and medical monitoring. The role combines scientific insight, regulatory expertise, and strategic oversight to help deliver compliant, patient-centric clinical solutions. Ideal candidates thrive in fast-paced, evolving environments, and bring both strong communication skills and a deep understanding of safety governance in clinical research.. . Accountabilities:. . Lead and manage the Safety team, serving as the primary point of escalation for all safety-related issues across clinical trials.. . Oversee execution of Clinical Event Committees (CEC), Data Safety Monitoring Boards (DSMB), and Medical Monitor reviews, ensuring consistency and regulatory compliance.. . Develop and review charters, safety narratives, and supporting documentation aligned with Good Clinical Practice (GCP), ICH, and protocol-specific procedures.. . Coordinate closely with internal stakeholders — project management, regulatory, biostatistics, and data management teams — to ensure timely preparation of meeting materials.. . Recruit and manage independent medical experts to serve on safety oversight committees.. . Provide clinical and operational support to the business development team during client engagements and proposals.. . Monitor project timelines and reporting metrics related to safety activities.. . Deliver process training to internal staff and contribute to continuous improvement initiatives.. . . Bachelor's degree in a health sciences discipline.. . Minimum 5 years of experience in clinical trial management, with at least 3 years focused on safety meetings and oversight.. . Strong knowledge of GCP, FDA regulations, and clinical project management best practices.. . Experience using Electronic Data Capture (EDC) systems and clinical trial management platforms.. . Proficient in MS Office applications; excellent communication and documentation skills.. . Ability to manage multiple projects, teams, and stakeholders effectively.. . Availability for 1–3 evening meetings per week depending on client scheduling.. . Proven ability to collaborate cross-functionally and maintain professional relationships with clients and committee members.. . Company Location: United States.