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 global biopharmaceutical company committed to making a meaningful difference in patients’ lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative TransCon® technology platform to fulfill our mission of developing new therapies that demonstrate best-in-class potential to address unmet medical needs.

At our headquarters in Hellerup, Denmark, research facilities in Heidelberg, Germany, and additional offices across Europe and the United States, we are advancing programs in our Endocrinology Rare Disease and Oncology portfolios. We also collaborate with partners on the development of TransCon-based products in 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 Clinical Trial Supply 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.

We evaluate applications when received, so we encourage you to apply as soon as possible. Please note that we conduct interviews on a rolling basis and reserve the right to remove the job posting at any time.

To ensure your application is reviewed, please submit it through the specified platform – applications sent by email or other channels will not be evaluated.

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

You can learn more about Ascendis by visiting our website

Applications must be submitted in English and will be treated confidentially.

A note to recruiters:

We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma HR team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs, your ownership of these candidates will not be acknowledged.