Jobs / Ferring Pharmaceuticals / Senior Clinical Trial Supply Manager

Senior Clinical Trial Supply Manager

Ferring Pharmaceuticals
Kastrup, Denmark Onsite Science & Medical Organization
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About this role

Job Description:

Senior Clinical Trial Supply Manager
Ready to help clinical trial supply reach patients worldwide?

Looking to make an impact in a global team driving clinical development success?

Come help us deliver high-quality clinical trial supply to trials all over the globe. At Ferring’s Global Clinical Trial Supply department we are looking for an experienced colleague to join our strong team of Trial Supply Managers, RTSM specialists and in-house Coordinators

Our International Pharma Science Center (IPC) in Denmark – Part of Ferring Pharmaceuticals
Ferring Pharmaceuticals is a global leader in reproductive medicine, maternal health, and key areas within gastroenterology and urology. By joining our International Pharma Science Center (IPC) in Kastrup, you become part of Ferring’s global network—collaborating across functions in a state-of-the-art waterfront building with stunning views of Sweden and easy access to Copenhagen Airport. You’ll work on-site with 550 highly skilled colleagues in an international, dynamic, and collaborative environment.
 

Ferring +You – Our collaboration

When you join us in Clinical Trial Supply, you get a team of 6 colleagues who care about and support each other. We preferably work in Trial Teams and have a high degree of interaction and collaboration within the department. We aim to have fun, and we expect that you will help maintain our good working atmosphere.

Your day at Ferring - Tasks where you are accountable
We are looking for a Senior Clinical Trial Supply Manager to ensure the timely and successful delivery of clinical trial supply to Ferring’s global development programs. In this role, you will lead supply strategy and execution for complex clinical trials, working closely with stakeholders across Clinical Development, CMC, Regulatory Affairs, Quality Assurance, and external partners.

As a senior member of the team, you will drive operational excellence, ensure compliance and supply continuity, mentor colleagues, and contribute to the ongoing development of our Clinical Trial Supply function.

Your tasks will be:

  • Lead Clinical Trial Supply Management for complex global clinical programs, ensuring robust supply strategies and successful trial execution.

  • Plan and deliver end-to-end clinical trial supply activities for Phase I–IV trials, including forecasting, sourcing, packaging, labelling, distribution, accountability, and destruction.

  • Act as the Clinical Trial Supply representative in cross-functional teams, driving alignment across Clinical Development, CMC, Quality, Regulatory Affairs, and external partners.

  • Manage suppliers and CMOs, including selection, contract oversight, performance management, and budget responsibility.

  • Ensure GxP-compliant execution through effective documentation, risk management, and oversight of key clinical supply records and systems.

  • Drive continuous improvement initiatives, provide subject matter expertise, and mentor colleagues to support capability building.

Behind our entrepreneurship … there´s your skills

Success in this role requires strong leadership and stakeholder management skills, a collaborative mindset, and a flair for operational excellence.

We are looking for an experienced profile with a strong background in Clinical Trial Supply.
 

We expect that you have:

  • Solid (more than 5 years’) clinical trial supply experience from the pharmaceutical industry.

  • Thorough knowledge of clinical trial operations, including drug development processes and regulatory requirements (GMP, GDP, GCP).

  • A proven ability to lead trial supply on large and complex projects independently.

  • Experience with supplier/CMO management and ownership of project-level budgets.

  • Strong communication and collaboration skills, with the ability to work effectively with different people and across cross-functional teams.

  • A proactive, flexible and improvement-minded approach.

  • An MSc in pharmaceutical or other relevant natural sciences.


Become a part of Ferring – apply now
If our mission and your vision are aligned, apply via the link in the job ad and include a short motivation in your CV.
Please note that we review applications on an on-going basis and we close the process when we find the right match.

Candidates must be located in the Øresund region as the position is onsite.

Note to agencies: This search is being managed by Ferring’s Talent Acquisition team. Kindly do not send us unsolicited profiles.


About Ferring Pharmaceuticals.
At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused in the areas of reproductive and women’s health, gastroenterology, and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. Read more at ferring.com.

Location:

Ferring Denmark

About Ferring Pharmaceuticals

Biopharmaceutical company focused on reproductive health, urology, and gastroenterology. Based in Saint-Prex, Switzerland.

ferring.com

Job Details
LocationKastrup, Denmark
Work typeOnsite
DepartmentScience & Medical Organization
SenioritySenior
CountryDenmark
About the company
Ferring Pharmaceuticals
Biopharmaceutical company focused on reproductive health, urology, and gastroenterology. Based in Saint-Prex, Switzerland.
View all 84 open jobs at Ferring Pharmaceuticals
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