We are pleased to announce that John Vemula joined Qserve Group as a part of our Qserve CRO team and works as a Clinical Data Manager based in the Netherlands.
John has worked as a Clinical Data Manager professional in Australia for about 3.5 years, and before that, he worked in India as a data and content management professional. Within Qserve, John will support clinical trials with his consistent and organized practices.
John: “As a Clinical Data Manager, I always aim to produce high-quality, reliable, and statistically sound data for Clinical Trials, which directly impact people’s lives around the globe. Working for Qserve as a CDM is always inspiring as they are the pioneers in assisting medical device and In-vitro diagnostics worldwide to achieve and maintain regulatory compliance. It is a pleasure to join a truly diverse organization with about 52 nationalities and seven offices worldwide.”
John’s profile is available on the website, explaining his experience and 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 guide manufacturers in gaining and maintaining compliance and 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 of combined expertise in the medical field. Teams in the EU, USA, and China provide 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.