Clinical Supply Chain Specialist
Vor 5 Tagen
As a Clinical Supply Chain Manager, you will play a crucial role in ensuring the smooth delivery of clinical trials within the pharmaceutical industry. Your primary responsibility will be to develop and implement optimal clinical supply strategies, working closely with cross-functional teams to achieve this goal.
Your Key Responsibilities:
- Represent GCS as a core member in the integrated Clinical Trial Team (iCTT), defining and advising on the optimal clinical trial supply strategy.
- Review overall clinical trial protocol/protocol amendments and provide inputs for developing optimal packaging design, clinical trial supply design, and visit schedule.
- Create and maintain complete and accurate clinical supply demand for assigned studies in alignment with protocol requirements and key study parameters.
- Develop and drive finalization of the packaging design and comprehensive label strategy for all participating countries in the clinical trial.
- Define clinical supply parameters for NIRT set up and initiate subsequent updates throughout the duration of the clinical trial.
- Develop and execute trial-level project plans together with relevant roles.
- Identify and assess supply risks to stakeholders and communicate appropriate mitigation strategies to ensure supply continuity.
- Collaborate with line function partners for country submission and approval timelines.
- Generate optimal distribution plans for investigational medicinal products.
- Develop an optimal resupply strategy with proactive planning and replenishment quantities.
- Consolidate and track the clinical trial budget with stakeholders.
- Contribute to the GCS subteam as a full member and exchange knowledge between teams.
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