National travel required, including to France and Belgium (French-speaking region)
Conduct on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits to ensure
Identify investigators and verify qualifications, resources, facilities, equipment and staff for
Train site staff as needed
Assist with regulatory/EC submissions when applicable

🎯 Requirements

Life Sciences degree or equivalent education/experience
Extensive on-site monitoring experience in phase 2/3 trials, ideally in oncology/rare diseases
Full working proficiency in English and French
Ability to plan, multitask and work in a dynamic team
Strong communication, collaboration and problem-solving skills
Willingness and ability to travel

🎁 Benefits

Join a specialist CRO focused on rare diseases and oncology
Collaborative, international team with opportunities across regions

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