Associate Director, Medical Writing

The Associate Director, Medical Writing will lead medical writing activities that support clinical development and regulatory submissions, working closely with clinical pharmacology, non-clinical, pre-clinical research, regulatory, and biostatistics external partners.

Requirements

• Minimum 10+ years of experience in early phase medical writing
• Strong project management skills and ability to deliver multiple documents on tight timelines
• Excellent written and verbal communication skills with attention to scientific detail
• Experience working in a global, matrixed environment and managing external vendors

Benefits

• Career advancement opportunities
• Meaningful impact and alignment with the company's mission
• Opportunity to work with a global biopharma company
• Inclusive and diverse work environment