Claire Borde has joined Qserve Group as a clinical writer where she is part of the Qserve CRO team. With her experience in Clinical Research, she will together with the other CRO team members, make a valuable contribution to our global customers. Claire is based in France.
Claire has over 13 years of experience in Clinical Research where she has worked in a different environment (investigational sites, sponsors, and CROs). She held various positions, such as site’s study coordinator in investigational sites, sponsor CRA in a big pharmaceutic laboratory, Studies Start-up/submissions specialist for France in big CROs, and Regulatory Affairs Project Manager for Medical Devices clinical trials in Europe.
Claire has a PhD in Transmissible diseases and tropical pathologies from the Faculty of Medicine of Marseille II, Marseille, France. She is a Certified Clinical Research Associate as well.
There’s a
personal profile available on this website where Claire explains more about her experience and her core competencies.
About Qserve GroupQserve’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 to support manufacturers or distributors of medical devices and in vitro diagnostics. Check our
current vacancies.