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- Approval of Certification Proposals for medical devices to be certified according to the Medical Device Regulation
- Performing assessment and preparing reports of clinical aspects of legal manufacturers technical documentation according to the requirements given in the Medical Device Regulation
- Evaluation of the summary of safety and clinical performance reports for high-risk medical devices
- Review and approval of clinical evaluation report and other relevant clinical documentation for accuracy and compliance with the requirements in the Medical Device Regulation
- Recommend for certification based on reviewed documentation
- Communication with the customers with regards to requirements, status and clinically relevant aspects
- Performing competence review of new resources (clinicians)
- Plan and execute assessment of clinical data as required, within agreed timescales and economic budget
- A competitive compensation and benefit package
- DNV training and qualification program
- A professional community in a prestigious technological company
- Possibilities to work with interesting and challenging projects
- Access to an extensive competence network
- Medical Doctor
- At least 2 years of working experience including: direct work experience in patient care research experience in conducting preclinical or clinical trials or assessing clinical data
- Strong written and verbal English communication skills
- Strong technical skills
- Analytical approach
- Good communication skills
- Customer focus
- Excellent reporting skills
- Ability to work independently and efficiently
- Ability to recommend on certification in complex cases
- A competitive compensation and benefit package
- DNV training and qualification program
- A professional community in a prestigious technological company
- Possibilities to work with interesting and challenging projects
- Access to an extensive competence network
Internal Clinician - London, United Kingdom - DNV
Description
DNV Product Assurance AS is one of the leading Notified Bodies for medical devices. The unit is entitled to carry out tasks related to conformity assessment of medical devices with EU Medical Devices Regulation before such products are placed on the market.
The role of Internal Clinician is to assess clinical data supporting safety and performance of devices.
Main tasks in this role are:
Personal Qualities:
We offer:
If you are interested, please submit your CV in English.