Global Regulatory & Site Start-Up Specialist
Listed on 2026-10-02
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Healthcare
Healthcare Compliance
Precision for Medicine is seeking a Regulatory and Start Up Specialist to drive site activation planning and regulatory submissions for clinical trials. You will prepare CTAs, compile dossiers, interact with authorities, and maintain trackers while coordinating with cross-functional teams to ensure timely startup across assigned sites and countries.
The ideal candidate has 1+ year of startup/regulatory experience in CRO or pharma, strong communication skills, and fluency in English.
We are seeking a motivated Global Regulatory & Site Start-Up Specialist to join Precision for Medicine in United States.
We have an opening for a Global Regulatory & Site Start-Up Specialist in United States within Management & Operations.
This role, Global Regulatory & Site Start-Up Specialist at Precision for Medicine, could be your next career step.
Are you ready to take on the Global Regulatory & Site Start-Up Specialist role at Precision for Medicine?
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