Clinical Trial Supply Manager

Are you passionate about clinical trial supply management? Do you have experience within GMP/GDP-regulated environments and managing complex clinical trial supply chains?
If so, now is your chance to join Ascendis Pharma as our new Clinical Trial Supply Manager.

Ascendis Pharma is a fast-growing global biopharmaceutical company committed to making a meaningful difference in patients’ lives. We have locations in Denmark, Germany, the United States, the UK, Italy, Spain, and France.

Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new therapies, selecting only those that demonstrate best-in-class potential to address unmet medical needs.

Today, we are advancing programs in Endocrinology Rare Disease and Oncology. In addition, we collaborate with partners around the world on the development of TransCon-based products for other therapeutic areas and markets.

We are seeking a passionate Clinical Trial Supply Manager to join our growing team. As a key member of the Ascendis Pharma team, you will play a crucial role in managing the clinical trial supply chain internally and externally. This is an exciting opportunity to work in a fast-paced environment, collaborating with cross-functional, global teams working together to achieve extraordinary results.

You will be joining the CTS coordination team in CTS consisting of 11 colleagues and report directly to Sara Østergaard, Director Clinical Trial Supply Coordination Team, who is based in Hellerup, Denmark. You will be based in Hellerup, Denmark.

Your key responsibilities will be:

• Coordinating internal CTS trial meetings and activities
• Collaborating with internal departments (CMC, Trial Management, QA, Regulatory Affairs)
• Forecasting, planning, and facilitating clinical supplies
• Managing IMP distribution from CMOs to clinical sites (Phase 1–3)
• Participating in Trial Team and Investigator Meetings
• Maintaining documentation in QMS and eTMF
• Reviewing and preparing trial-related instructions and manuals

Qualifications and Skills:

You hold a relevant academic degree – preferably a Master’s degree in Pharmacy or similar – and have 6+ years of experience within clinical trial supply management or in a GMP/GDP-regulated environment.

Furthermore, you have:

• Proven experience managing complex projects with multiple stakeholders
• Strong understanding of regulatory requirements
• Proficiency in Microsoft Office
• Fluency in English and Danish, both written and spoken

Key competencies:

You are a strong team player, analytical, and have a can-do attitude.
You possess an entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key. To succeed in this role, we also expect you to be collaborative, adaptable, and quality-focused.

Travel: 2–10 days per year

Office: Denmark, Hellerup, Tuborg Havn

Apply now.

Applications will be evaluated when received, so please apply as soon as possible.

All applications must be submitted in English and are treated confidentially.

For more details about the position or the company, please contact Sara Østergaard, Director Clinical Trial Supply PM Team at [email protected].

You can learn more about Ascendis by visiting our website www.ascendispharma.com

Applications submitted via email or other channels will not be reviewed.