Clinical Trial Supply Chain Manager

EPM Scientific; München; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading pharmaceutical company is seeking a Clinical Trial Supply Chain Manager to oversee global supply chains for clinical trials. The ideal candidate will hold a life sciences degree and have 2–3 years of relevant experience in a regulated environment, with strong communication skills and a team-oriented approach.

Qualifikationen

• 2-3 years of experience in a regulated environment (like GxP).
• Fluent in spoken and written German and English.
• Knowledge of clinical trial regulations (like GCP) is a bonus.

Aufgaben

• Design and manage global supply chains for clinical trials.
• Review production and packaging documentation in collaboration with teams.
• Support compliance with industry standards (e.g., GxP).

Kenntnisse

Problem Solving

Communication

Customer Service

Organization

Ausbildung

University degree in life sciences

Tools

Microsoft Excel

Jobbeschreibung

About us Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process? We have an exciting opportunity for you! Our Client a leading Pharma company is looking for a Clinical Trial Supply Chain Manager Tasks Key Responsibilities : Design and manage global supply chains for clinical trials across all phases (I–IV), working closely with internal teams to ensure smooth operations. Identify and monitor supply needs for clinical studies, including sourcing necessary materials and comparators, and manage related tasks in supply tracking systems (e.g., IRT), including system testing. Review production and packaging documentation , such as instructions, batch records, and standard procedures, in collaboration with quality, regulatory, and clinical operations teams. Ensure compliance with industry standards (e.g., GxP) by supporting the development of procedures and contributing to the ongoing improvement of supply processes for clinical trials. Represent the clinical supply function in interactions with internal and external stakeholders, and assist with supplier selection, contract management, and budget planning and tracking for assigned projects. Profile Required skills and qualifications : A university degree, ideally in life sciences (like biology or chemistry), plus some experience in logistics or a similar field, with clear results you can show. Around 2–3 years of work experience in a regulated environment (like GxP), preferably in areas related to medicine, research, or healthcare products. Good knowledge of rules in Europe and the U.S. for how clinical trial products should be labeled, packaged, and delivered. Knowing about clinical trial rules (like GCP) is a bonus. A team player who enjoys solving problems. Well-organized, flexible, and focused on getting results, with strong communication and customer service skills. Willing to travel internationally now and then (about 10% of the time). Comfortable using common computer programs, especially Microsoft Excel Fluent in spoken and written German and English Contact Please contact me on [e-mail] or please call me on [phone] for further information

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