d) – Medical Devices

Gi Group • biel, bern • Posted June 14, 2026

About the Role

Support the clinical strategy and clinical evidence generation for medical device products across their lifecycle. 
Plan, coordinate and/or oversee clinical activities, such as clinical investigations and other clinical evidence activities, including timelines, vendors/sites, documentation and quality. 
Prepare, review and maintain clinical and regulatory‑facing documentation (e.g., clinical plans/reports, study documentation, literature reviews, clinical summaries). 
Conduct or support systematic literature searches and evaluation of clinical evidence, including state‑of‑the‑art and benefit–risk considerations. 
Contribute to post‑market clinical activities and surveillance‑related deliverables (e.g., PMCF activities and reporting, inputs to PMS/PSUR where applicable). 
Support submissions and communications with relevant stakeholders (e.g., Ethics Committees, competent authorities, Notified Bodies), in collaboration with Regulatory A...
        