We are working with a leading international biopharmaceutical company to appoint a Clinical Trial Supply Lead. This role offers the opportunity to take ownership of global clinical supply operations, across all phases. You’ll work cross-functionally to develop and manage end-to-end supply strategies, while driving operational excellence and maintaining regulatory standards.
Key Responsibilities
* Design and execute global clinical supply strategies for Phase I–IV trials in close collaboration with internal stakeholders
* Forecast clinical supply needs and coordinate timely procurement of investigational products, comparators, and ancillary materials
* Oversee IRT system activities, including setup, updates, and user acceptance testing
* Review technical documentation such as packaging records, manufacturing instructions, and SOPs in partnership with QA, Regulatory, and Clinical teams
* Ensure full compliance with GxP regulations and contribute to the development and refinement of SOPs and best practices across the clinical supply function
Candidate Profile
* Clinical trial background within oncology
* Prior experience working in a GxP-compliant environment, preferably within pharma, biotech with exposure to clinical development processes
* Strong knowledge of EU and US regulations around the labeling, packaging, storage, and distribution of investigational medicinal products
* Effective communicator and problem solver, with the ability to work across global teams and manage multiple priorities
* Fluency in both German and English (spoken and written)
* Must be willing to travel onsite in Munich 2-3 days per week (Relocation support can be provided)
Please reach out to eireann.evans@meetlifesciences.com if you would like to discuss further.