Clinical Studies Coordinator in the pharma industry (M/F)

Reporting to the Director of Clinical Affairs, your main mission will be to implement and coordinate the execution of clinical studies on implantable products.

More specifically, you will:

Ensure the implementation of clinical studies:

• Design and/or write protocols and documents related to clinical studies
• Design case report forms
• Submit post-market ready clinical studies to the defined regulatory authorities (Competent Authorities, Ethics Committee, CNIL, etc.)

Coordinate and supervise the execution of clinical studies in compliance with regulations and deadlines:

• Select investigator sites and set up studies
• Select the subcontractors necessary for the execution of clinical studies
• Manage the administrative and regulatory aspects of clinical studies
• Monitor the proper progress of clinical studies (patient recruitment, follow-up visits, etc.)
• Control the quality of clinical studies

Ensure the completion of clinical studies:

• Close out sites
• Participate in the analysis and synthesis of data and write the final clinical study report
• Submit the necessary end-of-study documents to the competent authorities

Develop and write Department procedures in collaboration with the clinical team

Your profile:

Possessing higher scientific education (MSc, Engineer, etc.) ideally supplemented by a specialization in clinical evaluation or, you have 2-3 years of experience in writing clinical evaluation reports according to MEDDEV 2.7/1 rev4 or the European Medical Device Regulation 2017/745.

You are recognized for your clear, concise writing style with a high level of attention to detail. You possess the ability to understand, analyze, and interpret complex clinical data and have a strong ability to synthesize information, and you enjoy working in a team.

You demonstrate an ability to work in a demanding environment with tight deadlines and to perform multiple tasks.

Proficiency in operational English in writing is indispensable.

Daily essentials

• Company health insurance
• Meal vouchers and connected refrigerators
• Participation and Company Value Plan (PVE)
• Concierge service

*To learn more about this opportunity, we invite you to meet us at the Forum LNVDS on September 22, 2026, from 9:30 am to 4:00 pm in the Saint-Exupéry room, located at 155 rue des Écoles, 69730 GENAY. Access via the "Genay Lavoir" bus stop 43. Come in large numbers to discover our offers and exchange directly with the recruiters.*