Review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendments.
Works closely with Clinical Operations study teams and plays a key role to ensure deliverables are in alignment with defined study timelines.
Serve as a subject matter expert within the department and company regarding site contract management.

Graduate, postgraduate, 4-year college degree
Equivalent experience ideally in a scientific or healthcare discipline
Previous CRO experience
5+ years Oncology experience
Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements and site Budget negotiations, but no less than 7 years’ experience.
Experienced leading interactions with US/European/APAC or other regions institutions
Experienced leading interactions with Study Teams and Sponsor

Senior Contracts Manager – FSP

Key skills