Integrated Clinician

DNV GL

Arnhem

Hybrid

EUR 70,000 - 100,000

Full time

4 days ago
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Benefits offered by this job

Hybrid working
Pension plan
Professional development
Global profit share
Travel insurance

Job summary

DNV Product Assurance AS is seeking an Integrated Clinician to assess clinical data supporting the safety and performance of medical devices. The role involves MDR conformity assessment, evaluating clinical documentation, and communicating with customers. A Medical Doctor with clinical experience and strong English is required.

The position is part of the Life Sciences unit and offers a permanent contract with hybrid working options across locations including Arnhem, NL, among others.

Qualifications

  • Medical Doctor with at least 2 years of clinical experience.
  • Experience in evaluating clinical data or trials.
  • Strong written and verbal English communication skills.

Responsibilities

  • Approve certification proposals for MDR medical devices.
  • Assess and report clinical aspects of technical documentation as per MDR.
  • Plan and execute clinical evaluation assessments within timelines and budget.
  • Evaluate safety and clinical performance reports for high-risk devices.
  • Review clinical evaluation reports for accuracy and MDR compliance.
  • Communicate requirements and status with customers on clinically relevant aspects.
  • Perform competence reviews of clinicians and resources.

Skills

Medical Doctor
Clinical data assessment
English communication

Education

Medical Doctor degree

Job description

Integrated Clinician — the role of Internal Clinician is to assess clinical data supporting safety and performance of devices.

  • Locations: Oslo, Norway; Praha 6, Czech Republic; Stockholm, Sweden; Espoo, Finland; Gdynia, Poland; Hamburg, Germany; Anvers, Belgium; Amsterdam, Netherlands; Arnhem, Netherlands; Barcelona, Spain; Madrid, Spain; Milano, Lombardia, Italy; Piraeus, Greece; Hellerup, Denmark; Lisboa, Portugal
  • Business: Life Sciences
  • Position type: Full Time
  • Contract type: Permanent Employee
About us

We are the independent expert in assurance and risk management. Driven by our purpose, to safeguard life, property, and the environment, we empower our customers and their stakeholders with facts and reliable insights so that critical decisions can be made with confidence.

As a trusted voice for many of the world’s most successful organizations, we use our knowledge to advance safety and performance, set industry benchmarks, and inspire and invent solutions to tackle global transformations.

About Life Sciences

We help our customers in medical devices, healthcare, and aquaculture/ocean industries build trust and transparency across their products, assets, and supply chains. By working with customers to certify medical technologies, support safe and sustainable healthcare practices, and advance responsible aquaculture and ocean stewardship, we help manage risks, meet regulatory demands, and achieve long‑term goals. Drawing on deep technical expertise, we partner with customers worldwide to bridge trust gaps between patients, providers, producers, and consumers—driving sustainable results and improved ESG performance.

About the role

DNV Product Assurance AS is one of the leading Notified Bodies for medical devices. Unit is entitled to carry out tasks related to conformity assessment of medical devices with EU Medical Devices Regulation (MDR) before such products are placed on the market.

Main tasks in this role are:

  • Approval of Certification Proposals for medical devices to be certified according to the MDR
  • Perform assessment and prepare reports of clinical aspects of legal manufacturers technical documentation according to the requirements given in the MDR
  • Plan and execute the assessment of clinical evaluation, within agreed timescales and economic budget
  • Evaluate and validate 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 MDR
  • Recommend for certification based on reviewed documentation
  • Communication with the customers with regards to requirements, status and clinically relevant aspects
  • Perform competence review of new and existing resources (clinicians)
About you

Position Qualifications:

  • 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

Personal Qualities:

  • Strong technical skills concerning knowledge and experience with medical devices
  • Analytical approach
  • Good communication skills
  • Customer focus
  • Excellent reporting skills
  • Ability to work independently and efficiently
  • Team-oriented mindset
  • Ability to recommend on certification in complex cases
What we offer
  • 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
  • Social benefits as per DNV location (local conditions apply)
  • Global profit share scheme, depending on year-end results
  • Travel, life, and accident insurance
  • Pension and retirement benefits
  • Professional development through everyday tasks, projects, working with others, mentoring, and formal education
  • Hybrid Working: Adapting to the changing world of work around the world.
  • Opportunities to connect through social and professional networks
  • Flexible working hours and workplace, annual vacation allowance, competitive pension, insurance, and a global profit share scheme

Security and compliance with statutory requirements in the countries in which we operate is essential for DNV. Background checks will be conducted on all final candidates as part of the offer process, in accordance with applicable country-specific laws and practices.

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