VP of Regulatory Affairs - Leaman Life Sciences : Job Details

VP of Regulatory Affairs

I am partnered with a scientifically driven late-stage, well funded biopharmaceutical company who are looking to build out their Solid Tumors pipeline.

They are looking for a Vice President of Clinical Regulatory Affairs to be responsible for the development and execution of the company regulatory strategy, serving as global representative, leading and managing the clinical reg affairs function, including all aspects of clinical trial management, whilst supporting the coordination of all aspects of regulatory submissions.

This is a highly critical and visible role within the group, especially considering their short-term plans for commercialization.

Must have successfully led BLA or NDA submission/s.

This is a hybrid role, requiring at least 2 days a week in the office located in NYC

For more information contact [email protected] or click Easy Apply