Clinical Contract Specialist

Introduction:

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

Excelya - Excelling with care | European full-service CRO

Excelya is a European CRO offering full-service, customized solutions to perfectly match clients’ clinical research projects.

Key Activities :

• Within the contracts team, and in collaboration with other contract negotiators:
• Management of relations with hospital departments and hospital clinical research departments (DRCI).
• Negotiation of clinical research hospital agreements (Unique Contract)
• Preparation and validation of the initial additional costs grid with the project manager then with the trial coordinating site
• Application to associated sites
• Management of service contracts annexed to the tests (eg laboratories, loan of equipment, non-hospital specialized consultation, etc.)
• Update of the OSCARS database of additional costs

Profile :

• Experience in Clinical Research in a pharmaceutical laboratory, in international interventional clinical trials,
• Experience in written and oral negotiation with the DRCI for the discussion of unique convention grids,
• Knowledge of the clinical research environment, in particular the regulations relating to the Single Contract,
• Organization, rigor, dynamism, teamwork, negotiation skills, adaptability and good communication