CRA

​Responsibilities:

• 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

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Requirements:

• Scientific degree/education preferred

• Experience with monitoring in Belgium

• Fluent in English, French and Dutch

• Experience in CNS studies

• 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 – as required

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If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: roxanna.keshavarz@rbwconsulting.com / +44 1273 952187

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Salary: On application