Senior Clinical Trial Supply Manager
CK QLS are recruiting for a Senior Clinical Trial Supply Manager to join a growing biopharmaceutical company at their site based in Lausanne on a permanent basis.
Senior Clinical Trial Supply Manager Role: The responsibilities of this role will include:
- Managing the delivery of Investigational Medicinal Products (IMP) including Comparators/Standards of Care according to the study protocol and the project plan.
- Evaluating the feasibility and build a proposal for the supply of clinical trials in terms of packaging design, quality and regulatory compliance and supply chain.
- Managing the Contract Manufacturing Organization (CMO) performing the operational activities from packaging design to on site delivery, return, reconciliation and destruction.
- Estimating and defining a supply strategy with the CMC Project Leader and the Clinical Trial Manager (CTM).
- Setting up the packaging, labelling, storage and management of IMP with the internal (data management, CTM, ….) and external stakeholders (Contract Research Organization (CRO), CMO, Interactive Response Technology (IRT) vendors).
Your Background:
- Previous experience within Clinical Trial Supplies management for phase I to phase III international clinical studies (double-blind, comparator and standard of care sourcing).
- A broad understanding and experience in setting up (specification definition) of the main tools related to IMP management (simulation tools, IRT/Interactive Web Response System, …).
- Broad understanding of regulatory and Good Manufacturing Practices requirements for IMP supply.
- Project management skills, expertise of outsourcing.
- Fluent in English, French would be advantageous.
Apply: For more information or to apply for this Senior Clinical Trial Supply Manager position, please contact Jocelyn on 0041 (0) 782 516 595 or email jblackham@ckqls.ch, quoting job ref 48598.
Please send all of your correspondence in English.
It is essential that applicants hold entitlement to work in Switzerland.
