About this opportunity
ProPharma Group lists this Director, Medical Writing & Regulatory Strategy opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.