Senior Clinical Research Associate
ICON · New York, NY +3 more
Clinical OperationsFull-time$111k–$138kCompany career page
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Role summary
Senior Clinical Research Associate at a global clinical research organization supporting oncology trials across multiple northeastern US sites. Oversees site management, conducts monitoring visits, ensures regulatory compliance, and trains site staff. Requires 5+ years monitoring experience with at least 2 years in solid tumor trials, bachelor's degree, and up to 50% travel.
What they're looking for
- Bachelor's degree in scientific field
- 5+ years independent clinical trial monitoring with on-site and remote visits
- At least 2 years solid tumor oncology trial monitoring experience
- 1+ years early development trial experience
- Demonstrated site relationship development and compliance maintenance skills
- Expertise in GxP regulations and oncology-specific monitoring techniques
- Willingness to travel up to 50%
What you'll be doing
- Conduct remote and on-site monitoring visits including qualification, initiation, interim, and close-out activities
- Serve as primary liaison between sponsor team and clinical trial sites for efficient communication
- Manage essential document collection, TMF reconciliation, and regulatory inspection support
- Develop and implement corrective and preventive action plans based on identified root causes
- Lead site engagement initiatives and support site activation and feasibility assessment activities
Privacy & handoff
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