Clinical Supply Manager

Clinical Supply Manager

Your coordination and project management experience could be just what we need to help progress our fast-paced clinical trials. You will support global phase I-IV clinical trials from trial outline through trial close-out, giving you a broad portfolio and daily collaboration with a wide range of stakeholders.

Join a mid-sized, agile company where your work truly matters. You will collaborate across functions, tackle diverse challenges, and be part of a passionate team committed to advancing science and patient care.

Your new role

As our new colleague, you will support the progression of our R&D pipeline of promising drug candidates by taking ownership of clinical supply activities. You will coordinate clinical supplies for several clinical trials across phases, from initial trial design discussions through completion in close collaboration with external vendors and Lundbeck colleagues worldwide. In Clinical Supply, we are responsible for delivery of both small molecules and biologics IMP to the entire Lundbeck portfolio.

Your responsibilities may include defining outsourced CMO activities such as packaging, labelling, and distribution, as well as blinding strategies, supply forecasting, and depending on your interests, Interactive Response Technology (IRT). You will work independently on key assignments while being supported by a team of committed colleagues and encouraging leadership.

You can look forward to varied responsibilities across clinical trial and project-specific CMC deliverables, as we will be tailoring the challenges with your continued development. This role offers the opportunity to apply and enhance your project management skills, collaborate daily with stakeholders across functions and build specialized knowledge of clinical development.

Your future team

Clinical Supply in CMC currently consists of 10 highly skilled and passionate colleagues who are experts in coordinating outsourced packaging, labelling and distribution of Investigational Medicinal Product (IMP), as well as IRT-related activities. The team is composed of a balance of experienced professionals and newer members, ensuring a dynamic mix of deep expertise and fresh perspectives. 

You will be part of a dedicated and collaborative team with an open, trust-based, and supportive culture. We are energized by the complexity and pace of clinical trials and we value learning, respect and informal collaboration. We acknowledge each other and we believe that when we support each other, everybody succeeds.

We offer a position where you will contribute to the continued development of the clinical supplies area while growing your own experience and expertise. We value your dedication and are committed to supporting your professional development.

The position is based in Valby, Denmark.

Fully remote applications will not be considered. 

Applicants should be within commuting distance of Lundbeck’s headquarter in Valby.

What you bring to the team

You hold a master’s degree in pharmacy/engineering/chemistry/industrial medicine or similar.

We imagine that you have:

• 3-7 years of experience in Clinical Supply (IMP, IRT, Early Access), Clinical Development, Project Management, or related areas in pharmaceutical, biotechnology or medical device industry.
• Experience in clinical supply forecasting and supply planning
• Demonstrated stakeholder management skills, both internally and externally
• Experience in working with vendors and CROs / CMOs for clinical supplies
• Demonstrated problem-solving skills with the ability to prioritize, align, and simplify; used to manage multiple projects with changing priorities

You are inspiring and motivating in your collaboration with colleagues across cultures and organizations and have excellent coordination skills as well as a structured and analytical mindset. Furthermore, you are fluent in English, both written and spoken.

Our promise to you  

Lundbeck offers an inspiring workplace and innovative culture, where our curiosity, accountability and adaptability enable us to transform lives. We want to go faster and further on addressing the big unmet needs of people living with brain disorders. We offer rewarding careers with a mix of exciting tasks and development opportunities that are balanced with initiatives focused on your well-being.

We need every brain in the game, and at Lundbeck, we are committed to building a workforce that is as diverse as the people we serve. Read more about our commitment at .

Annual base salary range: 582 000 - 799 700 DKK gross

At Lundbeck, we are committed to fair and transparent pay. Please note that the final base salary within the stated range will be based on relevant qualifications, skills, competencies, and level of proficiency as well as internal pay equity. 

Apply now

Can you see yourself in this role? We want to hear from you. Does this sound like your dream job, but you’re not sure if you meet all the requirements? We still want to hear from you!

Upload your CV and include a few lines about your motivation for applying. We ask you not to include a photo or personal information that does not relate to your professional experience.

If you have questions, please contact Director Clinical Supply Dorthe Lerche Berg, Se e-mailadresse på jobs.lundbeck Vis telefonnummer until 17th July) or Senior Clinical Supply Specialist Malene Gantzhorn Pedersen, Se e-mailadresse på jobs.lundbeck .

Applications must be received by 9th August

Learn more about us at , LinkedIn or Instagram (@h_lundbeck).

#EveryBrainInTheGame

This job ad is intended for individuals seeking a career opportunity with Lundbeck. We engage with recruitment and search firms where needed on the basis of a written agreement, and we do not accept unsolicited requests of any kind. If you work as a recruitment consultant, you are kindly instructed to refrain from contacting Lundbeck or the hiring manager directly with suggested candidates. If you violate this policy, you do so at your own risk and for your own account, and Lundbeck will not assume any liability nor pay any associated fees resulting from such violation.