Clinical Research Associate - UK

I am working with a large CRO who are looking for a CRA II to work on a number of oncology studies across the UK.

This will be a home based role with no more than 15 visits per quarter as well as being single sponsor dedicated with a company car included.

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

Requirements:

• Minimum of 2 years’ experience independently monitoring in the UK
• Strong oncology background
• Bachelor degree in life sciences or similar field
• Knowledge of regulatory environment and guidelines (ICH, GCP, CFR, EU CT directive and local laws)
• Ability to travel, including overnight stays
• Ability to drive a car and have a valid driver’s license

If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail:

📞 01273 952187

📩 roxanna.keshavarz@rbwconsulting.com