CRA 2, Early Clinical Development
IQVIA · Carlsbad, CA +2 more
Clinical OperationsFull-time$90k–$150kCompany career page
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Role summary
IQVIA Biotech seeks a Clinical Research Associate 2 to monitor clinical trial sites and ensure protocol compliance, regulatory adherence, and data integrity. The role involves site management across multiple visit types, staff training, enrollment tracking, and regulatory documentation in early-phase studies.
What they're looking for
- Bachelor's degree in life sciences or health-related field
- Minimum 1.5 years of onsite monitoring experience
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements
- Ability to travel as required by assigned projects
- Early phase clinical development experience preferred
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits aligned with GCP and ICH guidelines
- Collaborate with site staff on subject recruitment strategies to meet enrollment timelines and goals
- Provide protocol training to site personnel and maintain ongoing communication
- Monitor protocol adherence, escalate quality concerns, and track regulatory submissions and data query resolution
- Maintain Trial Master Files and Investigator Site Files with essential regulatory documents
Privacy & handoff
This role links to IQVIA'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.