At IQVIA, I managed and maintained clinical and technical reference information for medical devices, supporting regulatory and medical information activities. I reviewed related documentation and helped ensure accuracy, consistency, and compliance with established procedures and quality standards.
In IQVIA's pharmacovigilance work, I processed and assessed adverse event cases for the Vaxzevria (AstraZeneca) project. I also performed quality control, deviation management, root cause analysis, and CAPA activities to support patient safety.
My experience also includes assisting healthcare professionals during medical examinations in a mobile medical unit and developing B2B sales for energy companies. I bring training in clinical and biomedical laboratory work, medical affairs, and key account management.
