Clinical Investigation expert
Wiebe Postma, PhD
Wiebe held a number of clinical positions in the Medical device industry. Wiebe holds 5 years of experience in Medical Device industries, specifically in Ophthalmology and Orthopedics. In his last position, Wiebe was responsible for clinical affairs at a large orthopedic manufacturer.
He designed, managed, analyzed and reviewed several clinical studies. Wiebe performed, as CRA, and coordinated the clinical monitoring process in compliance with GCP to assess the safety and efficacy of medical devices. As a junior expert, Wiebe has experience in planning and preparing clinical trials and development and review of study protocols, ICFs, CRFs, EC/IRB and regulatory submission.
Wiebe performed clinical auditing at international sites, as well as writing and maintaining clinical SOP’s and processes. Wiebe has experience collaborating with multiple disci¬plines located in different parts of an organi¬zation, using clinical regulatory requirements to develop effective clinical strategies. The following skills are considered critical: problem-solving, being analytical and focused on efficiency.
Wiebe combines strong experience in clinical research on an operational and managerial level with a practical, result-driven approach. He has acted as CRA and clinical study manager for a range of indications mostly in the field of orthopedic, ophthalmology, hematology, oncology diseases.
Wiebe about working at Qserve:
“I strongly believe in the value of a practical and user-friendly approach while ensuring a high standard of quality. I look forward to helping customers bring their products to the market efficiently in an increasingly demanding regulatory environment.”