Integrated Clinician

About the role

The Integrated Clinician will assess clinical data to support the safety and performance of medical devices under the EU Medical Devices Regulation (MDR). Working within DNV Product Assurance, the role involves reviewing technical documentation, communicating with customers, and contributing to certification decisions.

Key responsibilities

• Approve certification proposals for medical devices according to the MDR.
• Assess and prepare reports on clinical aspects of manufacturers' technical documentation.
• Plan and execute clinical evaluations within agreed timelines and budgets.
• Evaluate and validate safety and performance summaries for high‑risk devices.
• Review and approve clinical evaluation reports for accuracy and regulatory compliance.
• Recommend certification based on documented evidence.
• Communicate with customers regarding requirements, status, and clinical aspects.
• Perform competence reviews of clinicians and other resources.

Required profile

• Medical Doctor qualification with at least 2 years of relevant experience.
• Direct patient‑care experience and research experience in pre‑clinical or clinical trials.
• Strong written and verbal English communication skills.
• Technical knowledge of medical devices and analytical approach.
• Excellent reporting, independent work capability, and team‑oriented mindset.

What we offer

• Competitive compensation and benefits package.
• DNV training and qualification programmes.
• Access to a professional community within a prestigious technology company.
• Opportunities to work on interesting and challenging projects.
• Extensive competence network and location‑based social benefits.