Clinical Supply Project Manager
Key Responsibilities
- Lead and deliver clinical supply chain projects from initiation through close‑out.
- Act as the primary point of contact for sponsor/client communication, ensuring clarity around timelines, deliverable, risks, and overall project status.
- Ensure full adherence to GMP/GDP standards, international regulatory requirements, and internal SOPs.
- Conduct ongoing risk assessments and implement mitigation strategies to maintain smooth project progress.
- Oversee project materials, including stock management, shipments, recalls, and coordination of manufacturing‑related activities.
- Organise and lead project‑related meetings, including startup's, reviews, training sessions, and follow‑up on action items.
- Manage project budgets, financial forecasting, and invoicing cycles.
- Support vendor selection and ensure appropriate qualification for project needs.
- Participate in audits, inspections, and CAPA processes when required.
- Collaborate closely with Business Development, Quality, and operational teams to ensure seamless project delivery.
- Create, revise, and maintain project‑specific documentation and working instructions.
- Deliver or coordinate study‑specific training as needed.
Qualifications & Experience
- Bachelor's degree in life sciences, operations, business, or a related discipline.
- A minimum of two year's experience in clinical supply chain, pharmaceutical operations, or project management.
- Solid understanding of regulatory frameworks relevant to clinical supply (e.g., GMP/GDP, ICH guidelines, EU directives).
- Experience working with inventory management systems and technical equipment used within clinical logistics.
- Familiarity
If this role looks interesting to you, please do apply above and we will get back to you as soon as possible.
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