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Key Responsibilities:
- Review, draft, negotiate, and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements across various APAC locations.
- Actively take part in setting up contracting strategies for assigned projects and work closely with Clinical Operations study team to ensure deliverables are in alignment with defined study timelines.
Qualifications and Experience:
- Strong relevant experience in drafting, reviewing, and negotiating Clinical Trial Agreements and vendor contracts, as well as management, control, and tracking of the contract process within APAC region.
- Fully responsible for Site Contract Management from setting up site contracting strategy to execution of contracts, with strong site budget negotiation experience.
Working Environment:
- Proficiency in MS Office software programs and computer applications; handles sensitive issues with discretion.
- Works well independently and cooperatively with others to achieve common goals in a virtual environment; some domestic and occasional international travel including overnight stays.
Precision for Medicine
Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients. They have brought together new technologies, expertise, and operational scale to help the life sciences industry.