Senior CRA
ICON · Boston, MA
Clinical OperationsFull-time$111k–$138kCompany career page
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Role summary
Senior Clinical Research Associate in Boston overseeing clinical trial monitoring and site management at a large contract research organization. Role focuses on ensuring protocol adherence, regulatory compliance, and quality standards across multiple trial sites while leading and mentoring junior staff.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Extensive experience as Clinical Research Associate with deep trial process knowledge
- Ability to manage multiple sites and projects concurrently with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software systems
- Excellent communication and stakeholder management abilities
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard maintenance
- Conduct site visits to evaluate performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on accurate and timely data collection and reporting
- Train and mentor site staff and CRAs on clinical trial best practices and standards
- Establish and maintain relationships with site personnel to support trial execution
Privacy & handoff
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