Study Coordinator Arc Hospitalier H/F - 75

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work : our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.About the Job

Join Excelya, whereAudacity, Care, and Energydefine who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth GO hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main responsibilities :
- Carrying out the feasibility study and setting up the contributing centers
- Enter into the IT tool the data of patients with neuromuscular diseases newly included and followed up in consultation in all the contributing centers, in compliance with the inclusion criteria.
- Train contributors and users in the project and the IT tool
- Undertake to visit contributing centers according to a schedule defined by the scientific manager
- Identify evolving needs expressed by contributors
- Identify organizational bottlenecks in the centers involved, and propose solutions to ensure national representativeness of the patients included
- Contribute to the documentary database of the common IT portal dedicated to neuromuscular diseases
- Participate in the drafting of activity reports with project leaders, detailing project progress, meeting minutes, and database information documentation.
- Participate in project meetings (internal or external).
- Participate in patient information for studies using registry data.