Regulatory Submissions Lead | Veeva RIM Expert

A biopharmaceutical company in Watertown, Massachusetts is seeking an experienced Regulatory Operations Senior Submission Manager to manage investigational and marketing submissions. The ideal candidate should have over 7 years of experience in the biopharmaceutical/biotech industry, with significant expertise in Veeva RIM. Key responsibilities include monitoring submission timelines, maintaining regulatory compliance, and providing team training. Strong project management and communication skills are essential. Occasional travel may be required. #J-18808-Ljbffr