Clinical Trial Supply Chain Manager

Meet Life Sciences; München; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading international biopharmaceutical company is seeking a Clinical Trial Supply Lead to manage global clinical supply operations throughout all phases of trials. This role involves developing supply strategies, overseeing procurement processes, and ensuring compliance with GxP regulations while working collaboratively with various stakeholders. The ideal candidate should have a background in clinical trials, particularly in oncology, with strong knowledge of relevant regulations and proven communication skills.

Qualifikationen

• Strong knowledge of clinical development processes.
• Fluency in German and English, both spoken and written.
• Must be willing to travel onsite in Munich 2-3 days per week.

Aufgaben

• Design and execute global clinical supply strategies for Phase I–IV trials.
• Forecast clinical supply needs and procure investigational products.
• Ensure compliance with GxP regulations and refine SOPs.

Kenntnisse

Clinical trial background in oncology

Effective communication

Problem solving

Knowledge of EU and US regulations

Ausbildung

Experience in a GxP-compliant environment

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)