Clinical Trial Supply Chain Manager

Meet Life Sciences; Stuttgart; Vor Ort; EUR 70.000 - 100.000; Vollzeit

Zusammenfassung

A leading international biopharmaceutical company seeks a Clinical Trial Supply Lead to oversee global clinical supply operations. The role involves designing supply strategies for clinical trials and ensuring compliance with regulatory standards. The ideal candidate will have a clinical trial background in oncology and strong communication skills.

Qualifikationen

• Clinical trial background within oncology.
• Experience in a GxP-compliant environment, preferably in pharma or biotech.
• Knowledge of EU and US regulations for investigational products.

Aufgaben

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

Kenntnisse

Communication

Problem Solving

Project Management

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)