Senior CRA
ICON · New York, NY +1 more
The apply link worked recently (not employer-confirmed).
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
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.