Job description

Established in 2014, Excelya is a ‘people centered’ contract research organization (CRO).

We offer a personal and authentic experience within an ambitious young healthcare company on its way to becoming the leader in clinical research in Europe with our 800 Excelyates. Our unique one-stop-shop service model – leveraging a full-service, functional service provider and consultancy – allows our Excelyates to evolve across a wide range of projects. Working with leading experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.

For our team members, excelling with care means enjoying a challenging professional environment that encourages personal, intellectual and operational participation so that together we can be the best in our field. We are committed to empowering each Excelyate to express their natural talents, develop their full potential and invest in our unique project.



You will work on the launch and follow-up of clinical studies at the level of treatment logistics.

Study set-up:
– Proofreading the protocol and writing the treatment section
– Transcribing clinical data into treatment needs
– Organisation of the distribution (strategy)
– Creation of the treatment list

IRT set-up (IWRS/IVRS):
– Drafting of packaging and distribution specifications
– Setting up a study to define a procurement strategy for comparator drugs and device
– Participation in the drafting of documents: presentation, protocol, monitoring plan, pharmaceutical manual, instructions for use, etc.

Follow-up :
– Follow-up and interaction with the centres on their needs in terms of number of treatments
– Follow-up of the destruction of treatments at the end of the study


  • Organised and good interpersonal skills

  • Higher education (ideally Bac+5)

  • Experience in clinical research

  • Fluent English



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