Associate Director, Regulatory Affairs

Entrada Therapeutics is a clinical-stage biopharmaceutical company seeking an Associate Director, Regulatory Affairs to support global regulatory activities for its pipeline. The ideal candidate will collaborate with cross-functional teams to advance the global development of genetic medicines for rare and serious unmet medical needs.

Requirements

• BS or MS with at least 6+ years of increasing responsibility in Regulatory Affairs
• Demonstrated record of accomplishment, including support and execution of both US and global regulatory strategies
• Knowledge of the drug development process, GxP regulations, ICH, and FDA Guidance
• Experience with rare diseases, pediatrics, genetic medicines, or leveraging expedited development pathways

Benefits

• Comprehensive health, dental and vision coverage
• Life and disability insurance
• 401(k) match
• Paid, gender-inclusive parental leave
• Holistic support for your health and well-being
• Education reimbursement
• Discretionary time off
• Commuting benefits aligned to your working model