ProPharma Group is seeking a senior leader to head the medical writing and quality control function across clinical and regulatory documents for drugs, biologics, and devices. You will manage projects, budgets, and staff while building strong client relationships and leading cross-functional teams.
The role requires 7+ years of experience in medical writing/quality control, expert knowledge of regulatory standards, and the ability to drive process improvements in a fast-paced environment.
#J-18808-LjbffrDirector, Medical Writing & Regulatory Strategy in northern at Unknown Company
This position is listed as full time and onsite.