Clinical Research Associate - Sponsor Dedicated
IQVIA · Overland Park, KS +3 more
Clinical OperationsFull-time$90k–$190kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. Responsible for conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple study sites.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline preferred
- Minimum 1.5 years of on-site clinical trial monitoring experience
- Knowledge of Good Clinical Practice and ICH guidelines
- Proficiency with Microsoft Office Suite and standard computer platforms
- Strong written and verbal English communication skills
- Organizational and problem-solving abilities
- Ability to build effective working relationships with diverse stakeholders
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
- Develop and track subject recruitment plans with study sites to meet enrollment targets
- Provide protocol training and maintain communication with assigned sites
- Evaluate study site compliance with protocol requirements and applicable regulations
- Track study progress including regulatory submissions, enrollment metrics, CRF completion, and data queries
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.