Medical Device Clinical Evaluation Writer - CE Submissions & PMCF

Excelya; Lyon; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

A leading health company in Lyon is looking for an experienced Medical Writer focused on Clinical Evaluation for Medical Devices. This role involves developing clinical evaluation documentation, conducting literature searches, and supporting regulatory submissions. Ideal candidates should have a degree in life sciences, 2 years of related experience, and excellent writing skills. The company fosters an inclusive environment with a focus on quality, collaboration, and individual growth.

Qualifications

• Minimum of 2 years of experience in writing Clinical Evaluation Reports under MEDDEV or EU MDR.
• Ability to build comprehensive state-of-the-art summaries on pathologies and therapies.

Responsabilités

• Perform systematic scientific literature searches and critical analyses.
• Contribute to CE marking submissions and renewals.
• Write and update Clinical Evaluation Plans and Reports in line with MEDDEV 2.7/1 rev.4 and EU MDR 2017/745.
• Support Post-Market Clinical Follow-up activities.

Connaissances

Strong understanding of clinical research processes

Excellent writing and editing skills

Proficient in conducting literature searches

Attention to detail

Proficient in English

Formation

University degree in life sciences, biomedical engineering, or related field

Description du poste

A leading health company in Lyon is looking for an experienced Medical Writer focused on Clinical Evaluation for Medical Devices. This role involves developing clinical evaluation documentation, conducting literature searches, and supporting regulatory submissions. Ideal candidates should have a degree in life sciences, 2 years of related experience, and excellent writing skills. The company fosters an inclusive environment with a focus on quality, collaboration, and individual growth.