ICON seeks an experienced Senior Clinical Research Associate with oncology expertise to manage clinical trial sites across South England in a sponsor-dedicated partnership. The role involves monitoring site performance, ensuring protocol compliance, and collaborating with investigators to deliver high-quality studies.
Responsibilities
- Manage and monitor clinical trial sites across South England region
- Ensure protocol compliance, ICH-GCP adherence and regulatory requirement fulfillment
- Oversee site performance, data quality and study timeline achievement
- Build and maintain strong investigator and site team relationships
- Collaborate with cross-functional teams to support study delivery success
Requirements
- Previous CRA or Senior CRA experience with independent monitoring in UK
- Essential oncology clinical trial experience
- Strong ICH-GCP and clinical trial process knowledge
- Excellent communication, organisation and site-management skills
- Based in Southern England with regular site travel capability and valid driving licence
Vacancy posted 1 day ago
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