Clinical Research Associate 2, IQVIA
IQVIA · Durham, NC
Clinical OperationsFull-time$72k–$189kCompany career page
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Role summary
IQVIA seeks a Clinical Research Associate 2 to conduct site monitoring and management for clinical trials in CNS, metabolic, and cardiovascular therapeutic areas. The role involves monitoring visits, protocol training, data quality oversight, and regulatory compliance to ensure studies meet protocol and regulatory standards.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline preferred
- Minimum 1 year of on-site clinical trial monitoring experience
- Knowledge of GCP and ICH regulatory guidelines
- Proficiency with Microsoft Office Suite and standard computer systems
- Strong written and verbal English communication skills
- Organizational and problem-solving abilities
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
- Collaborate with sites on subject recruitment planning and tracking
- Deliver protocol training and maintain regular site communication
- Assess study site data quality, protocol adherence, and regulatory compliance
- Manage regulatory submissions, enrollment progress, CRF completion, and TMF documentation
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.