Since October 2021 Jorn van Binsbergen has joined the Qserve Group as clinical writer where he works within the Qserve CRO team.
Jorn about working at Qserve
I want to use my knowledge and skills to contribute to improving human health. I have experience in the medical device industry, where I previously worked for a manufacturer of orthopedic devices and implants. Now that I have joined Qserve, I am excited to expand my knowledge by working with different types of customers, where I will be mainly involved in the clinical evaluations of their devices. I look forward to further developing myself at Qserve working in clinical and regulatory affairs.
Before Qserve
Jorn obtained his bachelor’s and master’s degree in medical biology from the Radboud University in Nijmegen. During his master’s he chose a specialization track towards clinical biology and was always very interested in using fundamental knowledge of human physiology to improve human health.
After finishing his education, he decided to leave the academic environment to join the medical device community by taking on a job as quality engineer at a small medical device manufacturer. During his period working as a quality engineer, he gained a sound knowledge in both regulatory and quality affairs regarding medical devices.
As clinical writer within Qserve, he is involved in planning and preparing clinical evaluations, varying from writing clinical evaluation plans and reports and performing literature searches to preparing post-market clinical follow-up strategies and plans.
The key expertise areas of Jorn:
- Fundamental knowledge of the European Medical Device Regulation (MDR)
- Experienced in ISO 13485
- Strong scientific and technical writing
- Design and conduct systematic database searches, critical appraisal, and review of scientific literature
- Clinical evaluations of medical devices
- Sound knowledge in regulatory affairs
- Experienced in gap-analysis
- Knowledge of risk management
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Qserve CRO