Senior Clinical Research Associate
ICON · CA +3 more
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position at ICON overseeing Phase I Oncology clinical trial activities across West Coast locations. Role involves site monitoring, protocol compliance, and team leadership to ensure adherence to regulatory standards and successful trial execution.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with strong clinical trial process knowledge
- Proven ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management software
- Current Oncology monitoring experience
- Willingness to travel approximately 60%
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and mentor site staff and other CRAs on clinical trial conduct standards
- Build and maintain relationships with site personnel and stakeholders
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.