Meet Iris Verboven – Qserve's Business Operations Manager at Qserve CRO

At Qserve CRO, we are proud to have a team of highly skilled professionals dedicated to the success of clinical trials. Today, we are excited to introduce you to Iris Verboven, our CRO Business Operations Manager, whose practical approach ensures the most effective solutions for your clinical trials. 

Extensive Experience in Clinical Research 

With over 15 years of experience in the clinical research field, Iris knows what truly matters and understands your business perspective. She began her career in Business Development for a Notified Body, where she built a strong network within the Medical Device and IVD industry. 

Through her daily interactions with startups, mid-sized companies, and multinationals, Iris has developed a deep understanding of the operational challenges manufacturers face when managing clinical trials. Her proactive mindset, hands-on approach, and 24/7 availability enable her to address and solve issues quickly, ensuring that Qserve’s CRO operations run smoothly and efficiently. 

As Business Operations Manager, Iris brings a practical and results-driven mindset to every trial. Her expertise in budget control and liasion with Notified Bodies ensures clear and constructive communication, keeping studies on track while maintaining the highest standards of quality. 

A Strong European CRO 

Based in the Netherlands, Iris speaks several key European languages (Dutch, French, Italian, English, Spanish and German), enabling seamless communication with clients and our local CRAs across Europe. The Qserve CRO team possesses broad knowledge of country-specific requirements, ensuring that all aspects of your trial meet local and regional regulations. 

Every team member ensures full compliance while respecting agreed timelines and budgets — ensuring reliability and transparency in every project. 

Ensuring Success in Every Trial 

At Qserve CRO three core focus points for running successful clinical trials are: 

1. Ensuring full compliance with all regulatory requirements 
2. Respecting project timelines 
3. Managing budgets with precision. 

Partner with Qserve CRO for Your Clinical Trial Needs 

If you are looking to outsource the management of your clinical trial, Iris and the Qserve CRO team are here to support you. Whether you require full-service trial management or targeted support for specific study activities with proven experience in medical device and IVD trials. We are ready to help. 

Contact us today to learn how we can ensure the success of your clinical trial.