Qserve CRO is pleased to announce that Jorn van Binsbergen has joined our team to further expand his capabilities in supporting the clinical research organization for medical device and IVD’s industries worldwide.
Jorn van Binsbergen has joined Qserve where he is part of the Qserve CRO team and works as a clinical writer where he is involved in planning and preparing clinical evaluations, varying from writing clinical evaluation plans and reports. He also will performing literature searches to preparing post-market clinical follow-up strategies and plans.
He holds a bachelor and master’s degree in medical biology and chose a specialization track towards clinical biology and was most interested in using fundamental knowledge of human physiology to improve human health.
About Qserve Group
Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO and quality services.
Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing in medical devices. Check our current vacancies.