It is with pleasure that we introduce Wiebe Postma as a member of our expanding team of experts. Wiebe brings experience in clinical evaluation and clinical investigation (CRO) and will join us to strengthen the Clinical Evaluation Business area, supporting also the growing need for clinical data in the field.
Prior to Qserve, he worked at MicroPort as Clinical Study Manager EMEA. At MicroPort Wiebe was responsible for clinical affairs which included CRO management, clinical site assessment and qualification, developing protocols, investigator brochures, management of surgeon engagement, for studies in Belgium, Germany, France, Italy, Spain and UK.
Wiebe has a PhD in Biology with a strong emphasis on human immunology, virology, nutrition. During his studies he did internships and graduation studies at Mass General Hospital/Harvard Med School in Boston, and at the University of Freiburg, Germany.
Following his PhD, he started working as a Clinical Research Associate (CRA) at Ophtec, where he gained a lot of experience in the clinical evaluation and clinical investigation side of medical devices. In 2014 he spent a short intermezzo as CRA at Novartis, where he took part in management of phase I to IV pharmaceutical trials in hematology and oncology.
Anna Pietersma, Head of the Clinical Evaluation department of Qserve: “Wiebe will strengthen our quickly developing clinical team and work on Clinical Evaluations and Clinical Investigations (CRO)."
For more information, please see his profile.