Clinical Research Associate

I am working with a global CRO who is looking for an experienced CRA to join their CNS Team in Belgium.

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

Requirements:

• Scientific degree/education preferred
• Experience with monitoring in Belgium
• Fluent in English, French and Dutch
• Experience in one of the following indications: CNS, neurology, ophthalmology
• 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

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