Regulatory PM - IND/NDA Submissions for MedTech

A med-tech company based in Boone, NC is seeking an experienced Project Manager to lead IND preparation and submission for a medical device product. The ideal candidate will possess over 5 years of project management experience in the medical device, biotech, or pharmaceutical sectors with a strong understanding of FDA regulatory pathways. This hybrid role requires coordination with cross-functional teams and managing project timelines effectively. Competitive compensation and opportunities for professional growth are offered. #J-18808-Ljbffr