We are pleased that Iris Verboven returned to Qserve CRO to strengthen the clinical team in the role of business operation manager.
With Iris joining the Clinical team we have an experienced regulatory and clinical business developer as she gained experience working as a Sr. Business developer at BSi and Quinten MD (CRO in France). Iris is someone who always sees opportunities and knows how to set up large complex projects with a strong client-focused approach. Iris is pragmatic and speaks multiple languages.
The clinical operations team covers the Qserve CRO and the medical writing team. By bringing these teams together, customers can benefit from the broad clinical and regulatory knowledge within Qserve CRO. In addition, the regulatory knowledge from the medical device consultancy team, with a strong background in working at Notified Bodies, will be used to further support customers in developing strategies for clinical studies and clinical evaluations.
Are you looking for a full-service contract research organization for your medical device clinical trials with global coverage? Qserve CRO is an expert Contract Research Organization solutions provider specializing in medical devices and biotech.
In addition, the regulatory knowledge from the medical device consultancy team with strong backgrounds from working at Notified Bodies will be used to further support customers in developing strategies for clinical studies and clinical evaluations.
Want to learn more about what we could benefit for your company? Plan your introduction call with Iris.