Clinical Trial Manager

4 weeks ago


Culver City, United States Hamlyn Williams Full time

Key responsibilities for the CTM Include:


1. Supports and coordinates clinical trial activities and manages execution of 1 or more clinical trials/programs to ensure completion according to timelines.

2. Manage overall study timelines and oversight of the vendors deliverables.

3. Manage CROs and third-party vendors to ensure development and delivery of study documents, plans and manuals.

4. Assist and contribute to design of study materials such as assisting with development of IND submission documents, protocols/amendments, ICFs, patient diaries, and other study related materials.

5. Prepare, assist, and develop study plans such as monitoring manual, study operations manual, source data verification plan, pharmacy manual, and laboratory manual.

6. Coordinate study supplies

7. Responsible for oversight and project management of individual studies as well as relevant program related activities with minimal supervision including managing team meetings (Agendas, Minutes, Action Items, Follow Up).

8. Develop and review SOPs and processes, guidelines for compliance with global regulatory requirements.



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