Clinical Study Supply Manager – France

Excelya>All job opportunites>Full-time, Permanent Contract>Clinical Study Supply Manager – France

Job description

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.

We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model – leveraging full-service, functional service provider and consulting – allows our Excelyates to evolve through a diverse array of projects. In collaboration with preeminent experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.

For our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. We commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique project.

What we offer:

Working in the clinical operations department of a major laboratory based in Montpellier or Lyon,
you will work as a Clinical Study Supply Manager on the following assignments : 

  • The Clinical Study Supply Manager (CSSM) is responsible for the operational management of clinical supplies in a clinical trial.operational management of clinical supplies in a clinical trial.
  • The CSSM is responsible for ensuring that for each study he/she has under
    supplies are delivered on time, within budget and in compliance with the GXPs
    GXP, SOPs and standards.
  • The CSSM ensures the execution of clinical supply study activities
  • The CSSM is responsible for setting the best strategy for the study framework and
    and communicating with the study team.
  • He/she oversees a clinical supply production plan for a study
    and ensures progress according to study deadlines.
  • He/She reviews the strategy to optimise clinical supply chain and mitigate risk.
    mitigate risk.
  • He/she is the key contact for the Global Study Manager, as leader and expert for
    clinical supply activities.
  • He/she contributes to the review of the study documentation (Protocol, Monitoring Plan
    Monitoring Plan, Pharmacy Manual/Instructions for Use and ARC submissions).

 

 

Skills required :

  • You will have knowledge of clinical operations, if possible at global level.
  • The global context of the study requires a very good command of English.
  • Excellent communication and organisation skills
  • Mobility to Montpellier, Lyon or Paris
  • Rapid availability

 

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