• Responsible for evaluating clinical data for Medicontur’s medical devices, developing and updating documentation of clinical evaluation and post-market clinical follow-up, and
• Scientific and regulatory content writing
• Update clinical evaluation plans, clinical evaluation reports to assess safety and clinical performance clinical data;
• Perform post-marketing surveillance activities, review and write PMS documentation;
• Update PMCF plans and reports, summaries of safety and clinical performance;
• Conducts active PMS (e.g. PMCF surveys) activities;
• Develop clinical investigator brochures presented to regulatory authorities;
• Interfaces with risk management, R&D, regulatory affairs, study managers;
• Develop and update QMS procedures and document templates describing the clinical evaluation activities.

Please refer the Job description for details