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Years of Experience
Date Last Verified
ProfileLife Sciences Attorney The candidate will work on project based engagements. Should be a graduate of top tier law school with admission to practice in California. Must have 7+ years of experience in the pharmaceutical, biotechnology, medical device or similar industry. Should have extensive experience drafting and negotiating a wide range of agreements, such as clinical trial agreements, master services agreements, consulting agreements, manufacturing agreements, licensing and research collaborations; as well as agreements relating to the development, manufacture, supply and commercialization of therapeutics and diagnostics. Must have familiarity with and experience advising clients on compliance and regulatory matters, including FDA regulations (e.g. advertising, promotion and labeling), False Claims Act, Anti-Kickback Statute, OIG guidance, the PhRMA Code, HIPAA, Stark Law, Fraud and Abuse. Law firm and/or in-house experience is required.
Job ID: 18949
RGP (Resources Global Professionals)
695 Town Center Drive
Costa Mesa, CA 92626