Associate Project Director, Global Regulatory Affairs & Patient Safety
Ascendis Pharma
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Ascendis Pharma seeks an Associate Project Director to lead complex, cross-functional regulatory and patient safety initiatives across global operations. The role involves translating strategic priorities into execution plans, establishing governance frameworks, and coordinating stakeholders across multiple functions in a highly regulated environment.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workable, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Bachelor's or master's degree in life sciences, business, project management, engineering, or related field
- Minimum 8 years of pharmaceutical or biotechnology project management experience
- Demonstrated expertise leading complex, multi-functional projects in regulated environments
- Strong project governance, planning, and risk management capabilities
- Experience coordinating across regulatory affairs, patient safety, and clinical functions
- Proficiency in executive communication and stakeholder coordination
- Knowledge of GxP requirements and pharmacovigilance processes
What you'll be doing
- Lead GRAPS projects from initiation through closeout with defined scope, governance, and measurable outcomes
- Translate strategic priorities into integrated roadmaps and execution plans across regulatory and safety functions
- Establish governance forums, steering committees, and decision-making processes with executive reporting
- Coordinate cross-functional stakeholders across regulatory, clinical, quality, IT, finance, and external partners
- Drive process standardization and organizational scalability while maintaining GxP and regulatory compliance
Privacy & handoff
This role links to Ascendis Pharma's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.