Clinical Supply Chain Manager

EPM Scientific; Deutschland; Remote; EUR 60.000 - 80.000; Teilzeit

Zusammenfassung

A leading consulting firm is seeking an experienced Clinical Supply Chain Manager to join the team on a part-time basis for a 6-month project, overseeing critical operations in gene therapy trials. The ideal candidate will have at least 10 years of clinical supply chain experience, focusing on compliance and logistics for clinical trials. This remote role allows for flexible hours and requires a proactive, strategic thinker who is passionate about innovation in medicine.

Qualifikationen

• Minimum of 10 years of experience in clinical supply chain management within the pharmaceutical or bio-tech industry.
• Proven expertise in packaging, labelling, fulfilment, and logistics for clinical trials.
• Strong understanding of regulatory frameworks (FDA, EMA, MHRA) and GMP/GCP compliance.

Aufgaben

• Lead end-to-end clinical supply chain operations across multiple gene therapy trials.
• Oversee packaging, labelling, and distribution of IMPs in accordance with GMP and GCP standards.
• Manage relationships with CMOs, CROs, and logistics providers to ensure timely and compliant delivery.

Kenntnisse

Clinical supply chain management

Packaging and labelling expertise

Regulatory compliance knowledge

Project management skills

Communication skills

Jobbeschreibung

Job Title: Clinical Supply Chain Manager (Part-Time, 6-Month Contract)

Location: Remote - Germany / United Kingdom

Industry: Gene Therapy / Bio-pharmaceuticals

We are seeking an experienced Clinical Supply Chain Manager to join our team on a part-time basis for a 6-month project.

This role is critical to the success of our clinical programs, ensuring that investigation medicinal products (IMPs) are packaged, labelled, and delivered to clinical sites with precision, compliance, and efficiency.

Key Responsibilities:

• Lead end-to-end clinical supply chain operations across multiple gene therapy trials.
• Oversee packaging, labelling, and distribution of IMPs in accordance with GMP and GCP standards.
• Manage relationships with CMOs, CROs, and logistics providers to ensure timely and compliant delivery.
• Develop and execute supply chain strategies tailored to the unique needs of gene therapy studies.
• Monitor inventory levels, forecast demand, and mitigate supply risks.
• Ensure compliance with global regulatory requirements for clinical supplies.
• Collaborate cross-functionally with Clinical Operations, Regulatory Affairs, and Quality Assurance teams.
• Provide regular updates to project stakeholders and contribute to strategic planning.

Qualifications & Experience:

• Minimum of 10 year's experience in clinical supply chain management within the pharmaceutical or bio-tech industry.
• Proven expertise in packaging, labelling, fulfilment, and logistics for clinical trials.
• Strong understanding of regulatory frameworks (FDA, EMA, MHRA) and GMP/GCP compliance.
• Experience working with gene therapy or advanced therapy medicinal products (ATMPs) is highly desirable.
• Excellent project management and communication skills.
• Ability to work independently and manage multiple priorities in a fast-paced environment.

Contract Details:

• Duration: 6 months
• Commitment: Part-time (flexible hours negotiable)
• Start Date: ASAP
• Location: Remote London/ Germany

Join us in shaping the future of medicine. If you are a strategic thinker with a hands-on approach and a passion for innovation, we would love to hear from you.

To apply, please submit your CV above and our consultants will be with you as soon as possible!