Qserve CRO is pleased to announce that Aygül Dereli Öz has joined our team to further expand her capabilities in supporting the clinical research organization for IVD’s and medical device industries worldwide.
Aygül Dereli Öz has joined Qserve where she is part of the Qserve CRO team and works as a clinical project manager with experience in Clinical Research.
She holds a PhD degree in Molecular Biology, Master’s degree in Molecular Bioengineering and Bachelor degree in Molecular Biology and Genetics. She held a management position in Clinical Affairs Department in an international medical device manufacturer company. In this role she was responsible for designing clinical strategy and program to ensure compliance with Directives and Regulations. Moreover, she was responsible for execution of the preclinical studies including biological safety testing, assessments and animal studies.
Aygül has more than 10 years of scientific research experience (IVD research) and 6 years in Clinical Research in Medical devices.
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.