Senior Regulatory and Start Up Specialist (Argentina)
Precision Medicine Group · Other
Source: Himalayas
UTC -3 — no hybrid days in this listing.
This role’s source listing does not include Hungary as an eligible location.
Precision Medicine Group is hiring a Senior Regulatory and Start Up Specialist based in Argentina to manage clinical trial submissions and site activations.
The Senior Regulatory and Start Up Specialist will act as a Subject Matter Expert for clinical trial activities, including managing submissions to Competent Authorities and Ethics Committees. The role requires deep knowledge of local clinical trial regulations and experience in site start-up processes, budget negotiation, and maintaining audit readiness.
Why You’ll Love This Role
What You’ll Bring
What You’ll Get
About the Company
Precision Medicine Group is a specialized services and technology company that provides integrated clinical and commercialization solutions for the life sciences industry. The company focuses on accelerating the development and commercialization of new medical therapies.