Clinical Trial Supply Manager
vor 2 Wochen
For one of our pharma clients in Basel we are currently looking for a Clinical Trial Supply Manager for a 1 Year contract.
**Responsibilities**:
- Defines and advises on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency, and risk management
- Reviews overall clinical trial protocol/protocol amendments, provides inputs to develop optimal packaging design, clinical trial supply design and visit schedule
- Creates and maintains complete and accurate clinical supply demand for assigned study
- Creates and drives finalization of the packaging design and a comprehensive label strategy for all participating countries in the clinical trial
- Develops and executes a trial-level project plan together with all other relevant roles
- Identifies, assesses and proactively communicates supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
- Generates optimal distribution plans for investigational medicinal products
- Triggers and tracks shipments of IMPs from central depot to regional hubs and local depots
- Is responsible to consolidate, maintain and track the clinical trial budget with key stakeholders
**Profile**:
- Bachelor or University degree
- Analytical / critical thinking enjoying working with data and digital and attention to detail
- Fluent in English
- Basic project management, good organization, and planning skills
- Very good communication, negotiation, and interpersonal skills. Ability to work in interdisciplinary teams
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