Clinical Trial Supply Chain Manager

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

Zusammenfassung

A leading international biopharmaceutical company seeks a Clinical Trial Supply Lead. This role is crucial for managing global supply operations and ensuring regulatory compliance throughout various clinical trial phases. Candidates should have a strong background in clinical trials, especially within oncology, and excellent communication skills in both German and English.

Leistungen

Relocation support for onsite travel

Qualifikationen

• Experience in clinical trials, especially in oncology.
• Background in GxP-compliant environments, preferably pharma or biotech.
• Ability to manage multiple priorities and work across global teams.

Aufgaben

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

Kenntnisse

Clinical trial background

Effective communication

Problem solving

Knowledge of EU and US regulations

Fluency in German and English

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)