Clinical Research Associate - Sponsor Dedicated at IQVIA Carlsbad, CA

Clinical Research Associate - Sponsor Dedicated Job at IQVIA, Carlsbad, CA
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.
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

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

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