Clinical Research Associate, Sponsor Dedicated
IQVIA · Durham, NC +84 more
Clinical OperationsFull-time$72k–$189kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate responsible for site monitoring and management across multiple clinical trials. Ensures sites conduct studies in compliance with protocols, regulations, and sponsor requirements while managing recruitment, data quality, and regulatory documentation.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline preferred
- Minimum 2 years of on-site clinical trial monitoring experience
- Strong knowledge of GCP and ICH guidelines and clinical research regulations
- Proficiency with Microsoft Office (Word, Excel, PowerPoint) and laptop/mobile devices
- Excellent written and verbal English communication skills
- Strong organizational, problem-solving, and time management abilities
- Ability to build effective working relationships with sites and team members
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and close-out activities per protocol and GCP standards
- Collaborate with sites to develop and track subject recruitment plans aligned with project timelines
- Administer protocol training and maintain regular communication with sites regarding expectations and issues
- Evaluate site compliance with protocol requirements and applicable regulations, escalating quality concerns
- Track study progress including regulatory submissions, enrollment, CRF completion, and data query resolution
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.