At Qserve CRO, we are committed to delivering expert clinical trial management tailored to the unique challenges of the medical device and IVD industries. We are excited to welcome Daphne Smit-van den Hof to our team as a Clinical Project Manager, bringing extensive experience and a sponsor-focused mindset to support your clinical trial success.
Daphne joins Qserve CRO with a wealth of experience in clinical trial management, having worked for many years in the pharmaceutical industry. Her deep understanding of clinical trial operations from a sponsor’s point of view gives her unique insight into the budget constraints, regulatory hurdles, and strategic needs that manufacturers face.
Daphne’s career journey began in hospitals before she transitioned into the role of a Clinical Research Associate (CRA), where she honed her expertise in trial operations. Over the years, she has developed a comprehensive, full-service approach in project management, ensuring seamless execution of clinical trials across the Medical Device and IVD sectors.
Known for her straightforward, no-nonsense attitude, Daphne is a project manager who gets things done. Her clear communication style, problem-solving mindset, and hands-on approach ensure that trials move forward efficiently while maintaining compliance and quality. With a “Let’s see what’s possible” mindset, she is always looking for innovative ways to navigate challenges and streamline processes.
Daphne is based near Qserve’s headquarters in the Netherlands and is well-versed in the VEEVA eTMF, CTMS, and EDC systems that power our clinical trial operations. Her familiarity with these tools ensures a seamless integration with your clinical trial needs, providing sponsors with reliable support every step of the way.
Interested in learning more about Qserve CRO and how we can support your clinical trials? Schedule a free 30-minute consultation with Daphne and discover how her expertise can help drive your trial’s success.