Clinical Supply Chain Manager
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
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