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 perform site monitoring and management for clinical trials in immunology, gastroenterology, metabolic, dermatology, and respiratory therapeutic areas. The role ensures sites conduct studies in compliance with protocol, regulations, and sponsor requirements.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline, or equivalent education and experience
- Minimum 1 year of on-site clinical trial monitoring experience
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Proficiency with Microsoft Office (Word, Excel, PowerPoint) and mobile devices
- Strong written and verbal English communication skills
- Organizational, problem-solving, and time management abilities
What you'll be doing
- Conduct site monitoring visits including selection, initiation, ongoing monitoring, and close-out activities
- Collaborate with sites on subject recruitment planning and enrollment tracking
- Administer protocol training and maintain regular communication with assigned sites
- Monitor study progress including regulatory submissions, CRF completion, and data query resolution
- Maintain trial documentation and regulatory files in compliance with GCP standards
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.