Provide ongoing updates and support to project management
Demonstrate a commitment to quality in all aspects of monitoring and clinical research
Monitor Investigative Sites’ adherence to GCP, ICH guidelines and local regulations, and internal policies
Supervise the conduct of clinical studies, ensure compliance with protocols, regulatory requirements, and good clinical practice
Review, maintain and reconcile Trial Master Files against Investigator Site Files
Provide county-specific expertise to ensure operational compliance with local regulations
Work effectively with other departments and levels within the organisation
Minimum of 1 year experience as CRA
Scientific degree/education preferred
Background in medical and/or scientific knowledge preferred
Knowledge of regulatory environment and guidelines (ICH, GCP, CFR, EU CT directive and local laws)
Ability to travel extensively, including overnight stays
Fluent in French, Dutch, and English
Ability to work effectively across cultures
Ability 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: +44 1273 952187.
Salary: On application
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