Senior Clinical Research Associate
ICON · New York, NY +1 more
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
This role involves overseeing clinical trial monitoring activities for Phase I oncology studies across New York and New Jersey sites. The Senior CRA will manage site compliance with protocols and regulatory standards, conduct site visits, mentor staff, and coordinate cross-functional teams to ensure data integrity and trial execution. Requires a bachelor's degree in a scientific field, extensive clinical research experience, and willingness to travel approximately 60% of the time.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive clinical research associate experience with knowledge of trial processes
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in clinical trial software and relevant tools
- Excellent communication and stakeholder management abilities
- Willingness to travel approximately 60% of the time
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on accurate data collection and reporting
- Train site staff and other CRAs to maintain high standards of trial conduct
- Build and maintain relationships with site personnel to support trial operations
Privacy & handoff
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