Posted: 19 June
The role
Clinical Research Associate II (CRA II) – Oncology Focus | Multi-Sponsor Studies | UK Home-Based
We are seeking experienced Clinical Research Associates (CRA II level) to join a high-performing clinical operations team supporting multi-sponsor global clinical trials, with a strong focus on oncology studies.
This is a home-based role in the UK, offering national travel to sites across the country.
Key Responsibilities
- Conduct independent on-site monitoring visits (SIV, IMV, COV)
- Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements
- Support multiple concurrent studies across varied sponsors and protocols
- Perform source data verification, site training, and ongoing site management
- Maintain high-quality documentation and timely reporting in CTMS systems
- Build and maintain strong investigator and site relationships
Essential Requirements
- Minimum 1.5 years independent on-site monitoring experience in the UK (non-negotiable)
- Proven experience working as a CRA in a CRO or pharmaceutical environment
- Strong oncology clinical trial experience (critical requirement)
- Willingness to travel 8–10 days per month nationally
- Strong understanding of ICH-GCP and regulatory standards
- Excellent communication and stakeholder management skills
- Permanent right to work in the UK
- Comfortable managing multiple protocols and sponsors simultaneously
Desirable Experience
- Ophthalmology study experience
- Exposure to global / multi-regional clinical trials
- Experience across multiple therapeutic areas
- Strong progression towards Senior CRA responsibilities
