Clinical Trial Supply Chain Manager

ZipRecruiter; Gelsenkirchen; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading international biopharmaceutical company is seeking a Clinical Trial Supply Lead to oversee global clinical supply operations. This role requires a strong background in oncology and GxP compliance, with responsibilities including managing supply strategies and regulatory documentation. Ideal candidates will be fluent in both German and English, and able to work cross-functionally across global teams.

Leistungen

Relocation support

Qualifikationen

• Clinical trial background within oncology.
• Experience in a GxP-compliant environment.
• Strong knowledge of EU and US regulations for investigational products.

Aufgaben

• Design and execute supply strategies for Phase I–IV trials.
• Coordinate procurement of investigational products.
• Ensure compliance with GxP regulations.

Kenntnisse

Effective communication

Problem solving

Fluency in German

Fluency in English

Jobbeschreibung

Job Description

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 [e-mail] if you would like to discuss further.