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:
In collaboration with the project manager and clinical research associates:
– Administrative and budgetary activities for the various stages of a clinical trial (set-up, follow-up and closure)
– participation in project team meetings
– VeevaVault eTMF management: document loading and quality control of clinical trial documents
Minimum Requirements :
You have at least 2 years’ experience as a clinical trials assistant in a pharmaceutical company.
– Good knowledge of the Office package (Word, Excel, PowerPoint)
– Desired experience with eTMF (VeevaVault or similar)
– Experience or ability to adapt very quickly to system tools such as SAP/iBuy, CTMS VeevaVault, DocuSign….
– Team spirit, adaptability, ability to work on different projects at the same time and with different people
– Rigor and interest in quality control
The position is based in Paris Area
