Senior Clinical Trials Supply Manager

Are you ready to lead the end-to-end clinical trial supply from protocol input and IRT design to packaging/labelling and depot resupply Do you bring Clinical Trial Supply experience and want to shape scalable processes and budgets in a small high-impact team Will you thrive with partnering cross-functionally and with external vendors to deliver timely compliant clinical supplies We are looking for a Senior Clinical Trial Supply Manager to support increased level of clinical trials.

The position
The Clinical Trial Supplies team is part of Clinical Project Management in ALKs Global Clinical Development area. We are a small and dedicated team of enthusiastic and skilled professionals that has responsibility for managing clinical trial supply for ALKs clinical trials from early development phases to post approval phase.

As a member of the Clinical Trial Supplies team you will contribute to ALKs clinical development projects and be part of the clinical trial teams ensuring endtoend clinical supply planning and execution while ensuring timely compliant and patientfocused delivery of materials. The role offers broad crossfunctional exposure and the opportunity to influence how we scale our processes.

Key responsibilities in this role:

• Represent Clinical Trial Supply in Trial Teams and provide input to protocol design timelines and supply-critical decisions.
• Define and execute trial-specific supply strategies plans that ensure uninterrupted supply for patients across ALKs studies.
• Design secondary packaging and labelling including master and country specific label text planning and coordination of packaging operations to meet start-up and recruitment timelines.
• Participate in design and maintenance of trial specific IRT system (including setting of supply and resupply strategies monitoring of depot inventory levels).
• Participate in selection and oversight of ALKs external partners (CROs CMOs IRT providers).
• Build and managestudy supply budgets and forecasts.
• Develop and maintain regulatory/quality documentation (e.g. Product Specification Files SOPs work instructions).
• Ensure compliance with EU/US GMP GDP and GCP; manage deviations change controls and maintain inspection-ready documentation.

The position requires onsite presence at our HQ in Hørsholm (minimum 3 days/week). Some travelling is to be expected.

Your Profile
Your educational background and experience cover:

• Education: . in Pharmacy or a related scientific/technical discipline (e.g. pharmaceutical sciences biotechnology chemical or industrial engineering).
• Experience: minimum 3 years in Clinical Trial Supply within pharma/biotech with hands-on global study support from start-up through close-out; experience across early development to post-approval is a plus.
• Communication and stakeholder management: fluent in English; clear assertive communicator able to influence without authority and translate complex supply topics for diverse audiences.
• Ways of working: structured collaborative and pragmatic with a can-do attitude with high attention to detail and ability to prioritize across multiple concurrent trials.

Become a part of ALK
ALK provides a dynamic and pleasant work environment complete with inspiring and challenging assignments. The results of your efforts will be significant throughout the organization and you will be able to actively influence and challenge the status quo. Our flat structures attract independent individuals who like to feel the progress of the business and enjoy being close to the decision-making process. We prioritise an attractive working environment conductive to both professional growth and personal development. You will be part of an engaged and informal team who values skill and knowledge creation.

At ALK we are more than just a pharmaceutical company; we are a community dedicated to improving the lives of those affected by allergies. With over a century of leadership in allergy immunotherapy our commitment is to deliver the highest standards of patient care. Join our engaged team at our Head Office in Hørsholm located in the scenic DTU Science Park with green surroundings.

We believe that physical presence enforces strong teamwork collaboration and creates success so it is important that you enjoy coming to work at our site in Hørsholm with a degree of flexibility to also work from home.

How to apply
If you are excited about the prospect of driving impactful clinical development we encourage you to apply by attaching your CV and a short letter of motivation no later than 14 June 2026.

We commit to an inclusive recruitment process and equal opportunity for all our applicants. Hence we prefer that you do not add images to your application documents. We evaluate applications and call for interviews on an ongoing basis so dont wait to apply! We reserve the right to take down the advertisement when we have found the right candidate.

If you want to learn more about our company we encourage you to visit us at . For further information regarding the position please contact Head of Clinical Project Management Lisbet Bech Wreghitt at. We kindly ask us not to contact us with commercial inquiries.

We look forward to hearing from you!