Qserve CRO is pleased to announce that Dulce Aguilar has joined our team to further expand her capabilities in supporting the clinical research organization for medical device’s and IVD’s industries worldwide.
Dulce Aguilar has joined Qserve where she is part of the Qserve CRO team and works as a trainee clinical writer where she is involved in the clinical evaluation process, including literature search and appraisal, writing of clinical evaluation plans and clinical evaluation reports.
“It's nice to start at Qserve where I can also participate in the Young Talent Program that is especially aimed at starters. I'm really looking forward to it and I will work hard towards our goal of helping medical device manufacturers achieve their regulatory requirements.”
She conclude her PhD where her research was focused on developing an algorithm for the creation of 3D-printable vascular models for tissue engineering. With her strong technical background and expertise in diverse fields she can look at challenges from a broader perspective.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