Oncology CRA

​This will be a home based role and single sponsor dedicated with a company car included.

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Responsibilities:

• 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

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Requirements:

• 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

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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