Performs all types of monitoring visits: site qualification, site initiation, interim monitoring, site management and close-out visits
Adherence to GCP, ICH guidelines and local regulations, and internal policies across monitoring visits
Supervise the conduct of clinical studies, ensure compliance with protocols, regulatory requirements, and good clinical practice
Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness
Provide county-specific expertise to ensure operational compliance with local regulations
Work effectively with other departments and levels within the organisation
Scientific degree/education preferred
Experience with monitoring in Belgium
Fluent in English, French and Dutch
Minimum of 18 months experience required, working as a CRA
Ability to manage required travel of up to 75% on a regular basis
Able to drive a car and have a valid driver’s license
If you’re interested in finding more information about this role, please get in touch and I will be happy to discuss this further: email@example.com / +44 1273 952187
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