Overview
The Clinical Research Associate (CRA) will play a vital role in supporting clinical trials across the UK over a 12-month contract. This position involves collaborating with site staff, ensuring compliance with regulatory standards, and conducting various site visits. The contractor will work closely with a fast-growing Contract Research Organization (CRO) and will be expected to travel as required to meet project needs.
Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits.
- Ensure compliance with GCP, protocol, and regulatory requirements.
- Review source documents and CRFs for accuracy and completeness.
- Provide training and support to site staff.
- Prepare visit reports and follow-up letters.
Requirements
- Degree in life sciences or nursing.
- Minimum 2 years’ experience as a CRA.
- GCP certification required.
- Experience in oncology or rare disease trials preferred.
- Willingness to travel across UK sites.