Clinical Research Associate - Sponsor Dedicated
IQVIA · Overland Park, KS +3 more
Clinical OperationsFull-time$87k–$182kCompany career page
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Role summary
Clinical Research Associate supporting sponsor-dedicated clinical trials across multiple U.S. locations. Responsibilities include site monitoring, protocol training, recruitment tracking, data quality oversight, and regulatory documentation management to ensure protocol compliance and data integrity.
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 GCP and ICH guidelines for clinical research
- Proficiency with Microsoft Office (Word, Excel, PowerPoint)
- Strong written and verbal English communication skills
- 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 initiation, ongoing monitoring, and closeout activities per protocol
- Partner with sites on subject recruitment planning and tracking to meet enrollment targets
- Deliver protocol training to sites and maintain regular communication on project expectations
- Assess study site quality and regulatory adherence; escalate compliance issues appropriately
- Track study progress including regulatory submissions, enrollment, CRF completion, and data queries
Privacy & handoff
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