We're looking for a Clinical Trials Manager, working in the Biotechnology/Medical Devices industry in Foster City, California, United States.
Assists Clinical Program Manager in overall study management.
Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports.
Maintains study timelines.
Contributes to the development of the study budget.
Contributes to the development of RFPs and participate in the selection of CROs/vendors.
The pay range we're offering is 80 to 85 per hour. This position may present an opportunity to go permanent.
Our client is a people driven staffing company. Growing fast - 33% annually!
How? Building trusting relationships with top candidates. Like you! You’ll get one-on-one time focused on your skills, needs, and discovering opportunities in which you’ll thrive. The goal is to place you in the right position for you and your goals.
Where? Top IT and telecommunications companies. You’ll make a difference and grow in Technology, Government Services, Professional Services, or Engineering.
Helping you achieve your goals! It’s the right way and the only way to succeed in staffing.
Experience Required for Your Success
2 years of experience performing at the CTM level
Biotech/pharma experience required
Global phase 3 experience required
Inflammation experience preferable
Must be open to travel
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.