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.