Associate Clinical Supply Chain

Are you detail-oriented and experienced in (clinical) supply chain management? Would you like to work in an international environment supporting the setup of global clinical trials? Then this Associate Clinical Supply Chain position might be your ideal next step.

About the Role :

As an Associate Clinical Supply Chain, you will manage and execute clinical study setup processes within a regulated GMP, GDocP, and GDP environment. You will play a key role in supporting project managers to design and establish global supply chains, ensuring efficient and timely availability of investigational products for clinical trials.

Your work will involve system setup in SAP, handling master data, coordinating artwork and documentation, and collaborating with global stakeholders to support successful trial launches.

Key Responsibilities :

• Manage Master Data in SAP (Bill of Materials, WBS elements, custom values, etc.) to ensure readiness for clinical trials
• Coordinate and monitor artwork creation processes and resolve related issues
• Create and maintain the Product Specification File Study and third-party depot plans
• Support global supply chain setup activities and collaborate with cross-functional teams
• Track metrics and contribute to monthly workforce planning cycles
• Provide input for process improvements and ensure alignment with GxP guidelines

Who Are We Looking For?

We are open to candidates with experience in clinical supply chain or professionals from the biopharma / biotech sector who are ready to grow into this role.

Your profile :

What We Offer :

Interested?

Ready to make an impact in global clinical trials? Apply now and become part of a collaborative, patient-focused supply chain team.