Associate Director - Medical Writing

6 days ago

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Description

• Medical Writing serves as a strategic partner across drug discovery and development. • Authors a wide variety of regulatory documents independently, including complex submissions. • Participates in cross-functional teams for regulatory submissions and project teams. • May manage or supervise direct reports and contractors.

Requirements

• PharmD/PhD with 6+ years’ relevant experience, or • MA/MS/MPH/MBA with 8+ years’ relevant experience, or • BA/BS with 10+ years’ relevant experience. • Significant medical writing experience in the biopharma industry. • Proven track record in directing medical writing strategies. • Experience authoring a broad range of regulatory documentation. • Strong managerial abilities and knowledge of drug development process.

Benefits

• Company-sponsored medical, dental, vision, and life insurance plans. • Discretionary annual bonus. • Discretionary stock-based long-term incentives (eligibility may vary based on role). • Paid time off.

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