Emmes
Kathleen Peeters is an accomplished Clinical Research Manager with extensive experience in oncology, cardiology, and neurology. Currently, Kathleen holds positions at IBA as a Clinical Research Manager overseeing clinical study setups for Proton Therapy, and at Abbott as a Site Regulatory & Submission Associate focused on regulatory submissions for new studies in Belgium and the Netherlands. Additional roles include serving as a Pharmacovigilance Officer at Emmes, managing regulatory submissions and site management at NeuroScios GmbH, and coordinating Phase I trials at QPS Netherlands B.V. and Abbott. Kathleen's background includes significant involvement in both clinical study management and regulatory compliance across multiple therapeutic areas, supported by an educational foundation from KU Leuven and specialized training from HRD Academy.
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