Clinical Coordinator

TN France; Cagnes-sur-Mer; Sur place; EUR 40 000 - 46 000; Plein temps

Résumé du poste

A fast-growing company in aesthetic dermatology seeks a Clinical Research professional to manage post-marketing studies and regulatory submissions. Ideal candidates will have a Master's degree and experience in medical devices, with strong knowledge of ISO standards and fluency in English.

Qualifications

• 3 to 5 years of clinical experience in medical devices.
• Solid knowledge of ISO 14155 and MDR.

Responsabilités

• Set-up and follow-up of post-marketing clinical studies.
• Writing clinical documentation and handling regulatory submissions.
• Contributing to the scientific valorization of results.

Connaissances

Clinical Research

Cross-functional Collaboration

Project Management

Regulatory Knowledge

Formation

Master's Degree in Clinical Research

Biomedical Science

Regulatory Affairs

Outils

e-CRF Tools

Project Management Platforms

Description du poste

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Do you have experience in clinical research (sponsor side) and want to join an innovative company in aesthetic dermatology? This role is for you!

Join a fast-growing, internationally recognized company where scientific excellence and kindness shape the culture.

Your missions:

• ️ Set-up and follow-up of post-marketing clinical studies
• Writing clinical documentation & handling regulatory submissions
• Cross-functional collaboration with R&D, Quality, and Marketing teams
• Contributing to the scientific valorization of results

Profile sought:

• Master's degree in clinical research, biomedical science, or regulatory affairs
• 3 to 5 years of clinical experience (medical devices)
• Solid knowledge of ISO 14155 and MDR
• Fluent in English + familiar with e-CRF tools / project management platforms

Permanent role based in Cagnes-sur-Mer travel across France/Europe expected
Salary: 40-46K depending on profile