Keeps abreast of scientific, regulatory, and operational aspects for assigned projects.
Assists in site selection, initiation visits, and startup documentation.
May act as Feasibility Associate after training.
Conducts monitoring visits and ensures data integrity per protocol.
Performs source data verification and CRF data reviews.
Manages investigational products and study materials for supply.

🎯 Requirements

University degree in scientific medical or paramedical disciplines.
Previous proven CRA experience.
Strong knowledge of clinical trial operations, GCP/ICH.
Experience with infectious disease studies preferred.
Fluent in English and Dutch.
Proficiency in Microsoft Office (Word, Excel, Outlook).

🎁 Benefits

Global full-service CRO with 28+ years of delivery.
4,000 professionals in 20+ countries.
Equal opportunity employer.
Travel opportunities for project work.

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