Senior Clinical Research Associate
$110,520–$138,150 year
On-site · California, United States or Arizona, United States
Job Summary
Senior Clinical Research Associate responsible for leading site monitoring activities in oncology trials, ensuring protocol adherence, regulatory compliance, and high-quality data collection; conduct site visits, train site staff, collaborate with cross-functional teams, manage multiple sites, and drive timely trial execution; travel required (~60%) and employment contingent on legal right to work in the country.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Ability to manage multiple sites and projects simultaneously
- Proficiency in monitoring practices, data integrity, and site management
- Experience with relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Willingness to travel approximately 60%
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