Wouter Mattheussens has joined Qserve Group where he is part of the Qserve CRO team and works as a Clinical Project Manager. He is responsible for the setup, execution, and management of multiple clinical studies.
Wouter has studied Medical Biology with specialization Neuroscience and has coordinated clinical projects for an academic hospital where he gained experience and affinity with project management and ISO 14155/GCP-regulations.
He has a passion for contributing to the improvement of people’s quality of life by being directly involved in bringing new and existing medical devices to the market. With his background in the coordination of clinical projects he expands the CRO team with a strong helicopter view while keeping an out eye for nuance.
There’s a personal profile
available on this website where Wouter explains more about his experience and his core competencies.
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.