Length: Min. 6-12 months contract
The Clinical Trial Manager will plan and manage clinical trials including oversight of CROs, internal and external staff for the timely and quality implementation of trials.
Primary Responsibilities:
Perform CRO oversight activities such as Trip Report Review, TMF review, and co-monitoring visits, per Study Plans.
* Co-monitor studies
* Assist in the management of external vendors
Education/Experience/Skills:
Bachelors or Masters degree in a scientific discipline
9 years of related experience in life sciences
7 years of experience in clinical research
4 years of study management