Clinical Evaluation Consultant
Loes is part of the Clinical Affairs team and her area of expertise is in Clinical Operations. From protocol writing till EC submission, from site selection to trial report writing. Her main activities are to determine a tailored clinical strategy for high risk, class III products and delivering high-quality CRO services.
Loes about working at Qserve:
“Clinical operations require an eye for detail and flexibility. The variety of clients, devices, and activities keep me flexible and creative which makes it a very fun job!"
Prior to Qserve Loes worked as a CRA for a sponsor company, thereafter for a CRO. Activities in both roles included; study set-up, (inter)national site and CRO selection, protocol and essential document writing, (inter)national monitoring, site training, GCP training. Because of this experience, she can empathize with both the manufacturer and CRO.
To her opinion manufacturer and CRO functioning as an integrated team result in the most fruitful progress. The following skills are considered very useful: accurate, client-focused, communicative, both analytical and pragmatic.
Loes is GCP-certified and she has obtained a Master of Science in Medical Biology at the Radboud University in Nijmegen, the Netherlands.
Learn more about our services within Clinical Affairs