Job title: Clinical Supplies Manager
Location, Belgium, Germany, Netherlands
Key Responsibilities:
- Represents product supply in the Clinical Study Team, driving the development of tailored clinical trial supply strategies aligned with the relevant clinical trial protocol.
- Creates and maintains complete and accurate clinical supply demand for clinical studies, aligning with protocol requirements, key study parameters, milestones, and patient projections.
- Manages IRT set-up, conduct, and close-out from a clinical trial supplies perspective, and develops and executes detailed clinical trial supply project plans in collaboration with stakeholders, ensuring compliance with GxP requirements, local regulations, and internal processes.
- Develops study-specific pharmacy manuals and other relevant guides in collaboration with the Clinical Study Team and CMC team, actively tracks drug inventory, and visualises active drug consumption versus projected forecast.
- Contributes to planning and organisation of global product manufacturing activities, provides logistics support to the manufacturing team, and manages external clinical trial supply vendors and distributors.
- Collects, registers, and archives information and documents in accordance with applicable GxP guidelines for clinical studies (TMF, eTMF), and consolidates, maintains, and tracks the clinical trial budget.
Key Requirements
- Experience managing contracts and budgets
If this role feels like the perfect match for you, seize the opportunity and apply today!
