Clinical Trial Supply Manager

About the role

Ascendis Pharma is seeking an experienced Clinical Trial Supply Manager to lead supply chain activities for Phase 1‑3 studies. Based in Hellerup, Denmark, you will work within a fast‑paced, cross‑functional environment supporting our endocrine, rare disease and oncology programs.

Key responsibilities

• Coordinate internal CTS trial meetings and collaborate with CMC, QA, IT, Regulatory Affairs and Trial Management.
• Forecast, plan and facilitate the supply of investigational medicinal products (IMP), including packaging design, labeling and packaging runs.
• Manage IRT setup, specification, UAT, go‑live, close‑out and post‑go‑live changes.
• Oversee IMP distribution to clinical sites and direct‑to‑patient shipments, handling temperature excursions and drug accountability.
• Maintain documentation in QMS and eTMF, preparing trial‑related instructions and manuals.

Required profile

• Relevant academic degree in pharmacy or related field.
• Minimum 5 years experience in clinical trial supply management within GMP/GDP‑regulated environments.
• Proven project management skills with multiple internal and external stakeholders.
• Strong understanding of regulatory requirements.

Required skills

• Proficiency in Microsoft Office.
• Fluency in written and spoken English and Danish.