Clinical Research Associate 2, IQVIA
$71,900–$189,000 year
On-site · Durham, North Carolina, United States
Job Summary
Clinical Research Associate 2 at IQVIA performs site monitoring and site-management activities to ensure compliance with the study protocol, GCP/ICH guidelines, and sponsor requirements. Responsibilities include conducting site monitoring visits (selection, initiation, monitoring, and close-out), driving subject recruitment plans, administering protocol training to sites, evaluating site practices for protocol and regulatory adherence, tracking regulatory submissions and data entry (CRF, TMF/ISF), generating visit reports and follow-up communications, and collaborating with study-team members. May support start-up activities and site financial management as applicable. Required skills include strong knowledge of GCP/ICH, experience with on-site monitoring and CRFs, and excellent written/verbal communication and organizational abilities.
Required Qualifications
- Bachelor's Degree in scientific discipline or health care preferred
- Requires at least 1 year of on-site monitoring experience
- Good knowledge of GCP and ICH guidelines
- Computer skills including Microsoft Word, Excel and PowerPoint
- Written and verbal communication skills in English
- Organizational and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
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