Descrição
Associate Clinical Trial Supply Manager
My Client who is one of the biggest Pharmaceutical Companies in the world are looking for an Associate Clinical Trial Supply Manager to join their team on site in Basel, Switzerland. They are offering a 1 year contract at a 80-100% workload with an option of extension! They have a huge amount of drugs in the pipeline giving you longevity in your contract and ability to learn new skills! Although this is a contract position our client looks for long term collaboration allowing for promotions all while benefiting from working as a contractor!
Some of the responsibilities:
Represents Global Clinical Supply (GCS) as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT 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.
Develops and executes a trial-level project plan together with all other relevant roles.
Actively contributes to the GCS sub team as a full member. Ensures adequate, proactive exchange of relevant knowledge & information between the GCS sub team and the CTT.
Requirements:
Bachelor or University degree
Previous experience in Clinical Trial Supply
Analytical / critical thinking enjoying working with data and digital and attention to detail
Project management, good organization and planning skills
Fluent in English
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