KLIFO Clinical Trial Supply (CTS) is looking for an experienced Clinical Supply Manager to strengthen our team.
At KLIFO, you will work closely with experienced specialists in a flexible working environment. Together, we help clients in the life science industry plan and execute robust clinical supply solutions across different therapeutic areas.
The position is located at our office in Brøndby, Denmark.
Become part of an experienced and dedicated team
As a Clinical Supply Manager, you will have a central project manager role in the management of complex clinical studies and you will act as a strategic sparring partner for our clients. You will work closely with both internal and external stakeholders to ensure robust solutions, efficient execution, and high client satisfaction.
You will become part of a well-established team of 27 experienced and committed colleagues, characterized by strong expertise, close collaboration, and a culture defined by responsibility, trust, and quality.
As a Clinical Supply Manager, you will contribute by:
- Planning and coordination of clinical studies with a focus on structure, timelines and quality
- Close and proactive client dialogue, providing advice based on experience and a solid overview
- Design and approval of packaging solutions and blinding strategies in accordance with GMP and regulatory requirements
- Preparation and approval of label texts
- Close collaboration with packaging, distribution, QA, warehouse, and other internal functions to ensure timely and accurate delivery of clinical trial supplies
- Active use of IRT as an integrated part of the clinical supply strategy, including:
- Inventory management, randomization, supply strategy, and distribution to clinical sites
- Preparation of requirements specifications, testing, validation, and implementation of IRT systems (e.g., IXRS or equivalent)
Your background and qualifications
We are looking for an experienced profile who combines strong professional expertise with a positive mindset and a desire to work closely with others. You naturally take on responsibility, you act structured and professional, and at the same time contribute to a culture where collaboration, trust, and job satisfaction are key elements.
In addition, we expect that you:
- Have solid experience within clinical trial supply; experience with IRT systems is a clear advantage
- Have in-depth knowledge of GxP and regulatory requirements
- Are a strong project manager who can handle complexity and multiple stakeholders without losing overview
- Thrive as a team player and actively contribute to a positive and informal working environment
- Communicate confidently in both Danish and English, written and spoken
Why work at KLIFO?
- Become part of an organization where employees and their expertise are our most important asset
- Enjoy a flexible workplace with a culture built on trust, transparency, and respect
- Work alongside some of the most experienced and dedicated colleagues in the life science industry
- Contribute your expertise across a wide range of therapy areas
- Help develop tailored solutions based on cross-functional collaboration
- Build mutually valuable relationships with our customers
- Be part of an organization that sees knowledge sharing as the path to success
Application deadline
Please send your application to job@klifo.com and mark it “Clinical Supply Manager” no later than 16 January 2026. Please also state where you saw this job posting. Interviews will be conducted on an ongoing basis.
If you have any questions about the position, please contact Lotte Harreby, Director, at lotte.harreby@klifo.com or +45 44 222 969 for further information.
KLIFO will use your application and related personal data solely for the purpose of managing this specific recruitment process. All personal data will be handled confidentially in accordance with the General Data Protection Regulation (GDPR). For information about KLIFO’s processing of personal data, please visit www.klifo.com.
