Sr CRA - Oncology experienced required
On-site · Reading, England, United Kingdom
Job Summary
Senior Clinical Research Associate (CRA) responsible for monitoring clinical trial sites to ensure protocol adherence, regulatory compliance, and GCP. Responsibilities include site visits to assess performance, issue resolution, cross-functional collaboration for data collection and reporting, and providing training to site staff. Must have 7+ years as a CRA with oncology experience, strong site management and data integrity skills, proficiency with clinical trial software, and excellent communication and stakeholder management. Travel at least 60% (international and domestic) with a UK base required; role supported by sponsorship. Employment with ICON contingent upon legal right to work in the UK.
Required Qualifications
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- 7+ years' minimum experience as a CRA
- At least 2 years' experience on Oncology studies
- Ability to travel at least 60% (international and domestic)
- Valid driver’s license may be required
- Employment with ICON contingent upon legal right to work in the country where the role is based
Additional Requirements
- Based in the United Kingdom
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