At Qserve CRO, we’re proud to work with a dedicated team of clinical research professionals who are committed to delivering high-quality, compliant, and efficient trial services. Today, we’re pleased to introduce you to Wouter, one of our experienced Clinical Project Managers, whose expertise plays a key role in the successful execution of complex clinical trials.
Wouter joined Qserve three years ago, bringing with him valuable experience from managing trials in academic hospital settings. These high-paced environments demanded agility—balancing budgets, ensuring compliance, and making fast, informed decisions. This background shaped his pragmatic, solution-driven approach to trial management, making him a vital asset to our CRO team.
Wouter is known for focusing on solutions rather than limitations. He approaches challenges with a mindset geared toward finding options and driving efficiency. Thanks to his hands-on style and adaptability, he has successfully managed large international trials with precision and care.
Based in the Netherlands, Wouter works closely with our regional CRAs and site coordinators. His strong knowledge of ISO 14155, MDR 2017/745, and experience with various EDC platforms further strengthen Qserve CRO’s capabilities in regulatory compliance and clinical operations.
If you’re looking for a trusted partner to manage your clinical trial with precision and reliability, Wouter and the Qserve CRO team are here to support you. Whether you need end-to-end trial management or help with specific components, we’re ready to help you move your study forward. Efficiently, compliantly, and with a personal touch.
Get in touch with us today to learn how we can support your clinical trial goals.