Tasks & Responsibilities

• 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–. 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),...