Associate Director, Medical Writing

The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company’s drug development programs. The ideal candidate will have deep experience in regulatory medical writing and regulatory operations, exceptional attention to detail, and the ability to collaborate effectively with cross-functional teams.

Requirements

• BA, BS or advanced degree in life sciences, pharmacy, or a related field
• 5+ years of experience in regulatory medical writing within the pharmaceutical or biotech industry
• In-depth knowledge of global regulatory requirements, guidelines, and the drug development process

Benefits

• Medical, dental, and vision insurance
• 401k match
• Unlimited PTO
• Paid holidays, including winter shutdown