The Company is seeking an Interim VP, Regulatory Affairs to join their team. The successful candidate will be responsible for providing senior strategic and hands-on support in setting regulatory priorities across development programs, leading the preparation for FDA interactions and key submissions, advising cross-functional teams on regulatory decisions, and providing oversight to ensure the progress of work during a period of limited team capacity. This role is pivotal in the advise-build-operate model, contributing to the de-risking and acceleration of high-profile drug and device programs. Applicants for the Interim VP, Regulatory Affairs position at the company should have a strong background in regulatory affairs, with the ability to lead and influence in a dynamic and fast-paced environment. The role requires a deep understanding of regulatory sciences, clinical research solutions, quality and compliance, pharmacovigilance, medical information, and R&D technology. The ideal candidate will have a proven track record in a similar senior role, with the capacity to provide strategic guidance and hands-on support. A collaborative and innovative approach is essential, as is the ability to work with diverse teams and clients. A minimum of 20 hours per week is expected, with a hybrid work schedule and minimal travel.

Hiring Company

ProPharma Group