Clinical Trial Assistant

I - Excelya : 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. To learn more about us, visit www.excelya.com II - Clinical trial Assistant • Provide administrative and regulatory support for clinical trials(protocol, observation books,submission documents) • Management of replenishmentdelivery of medical products to pharmacies • In charge of preparing and sending documents to the centers • Collaboration with partners and subcontractors identified on pro-jects • Financial tracking • Responsible and exchanges with foreign CRAs for the cleaning of TMF: Validation of regulatory documents, validation of the certificate archiving, adaptation of the TMF tracker. Responsible for harvesting latest regulatory documents CRFs and SEQs validation pages. • Sends a list to the CRAs of theregulatory documents to be collectedor corrected. Upon receipt of theclosing documents, return to the ARCsif there are errors and missing docs.Help the CRAs to finalize the closingsby contacting the centers and send a closing letter and follow up. Deactivation of pharmacist accounts • Bibliographic search, Writing the research protocol and analysis plan • Establish the data collection tool III - Minimum Requirements : Diploma or University graduate with a Life Science degree Fluency in English (Written and spoken) Prior experience in experience in the clinical research area is a big plus

Location: Paris, FR

Posted Date: 1/14/2025