Robert Majoie is a Clinical Research Professional with over eight years of experience in start-up processes across various clinical trials and therapeutic areas. Currently serving as a Principal Country Approval Specialist at PPD, Majoie previously held roles including Senior Study Start Up Associate at ICON plc and Study Start Up Associate II, where responsibilities included site initiation, preparation and submission of clinical trial applications, and training new colleagues. Majoie also gained valuable experience as an intern at RIVM, contributing to advisory projects related to the National Vaccination Programme. Majoie holds a Master’s degree in Medical Pharmaceutical Sciences and a Bachelor’s degree in Life Science & Technology from Rijksuniversiteit Groningen.
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