Clinical Trial Supply Chain Manager

Sei unter den ersten Bewerbenden.
Nur für registrierte Mitglieder
Stuttgart
EUR 70.000 - 100.000
Sei unter den ersten Bewerbenden.
Vor 3 Tagen
Jobbeschreibung

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)