Local Study Manager – France

Excelya>All job opportunites>Full-time, Permanent Contract>Local Study 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:

In a national and international context, you will be involved in setting up, monitoring and closing clinical trials in the field of oncology, working with the teams of one of our customers, one of the world’s largest pharmaceutical companies.
You will be responsible for coordinating the local clinical team. You will be involved in
– Preparation of clinical study documents
– Management of the study schedule and budget.
– Selection and management of centers and subcontractors.
– Coordination of all activities to ensure patient recruitment.
– Provision of study results under optimum conditions of quality, timeliness and cost.
– Management of regulatory submissions and administrative follow-up in compliance with legislation, GCP and internal procedures.
– Feasibility studies, selection of investigators
– Operational management of a team of Clinical Research Associates.

Minimum Requirements :

– At least 3 to 6 years’ experience in the pharmaceutical industry, in the operational and budgetary management of international interventional clinical trials.
– Experience in the field of oncology or tumor biomarkers
– Organized, dynamic, good communicator, team player, leader
– Good English and scientific skills



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