Clinical Research Associate - Sponsor Dedicated
$87.2k - $182kIQVIA
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.
Responsibilities
- 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
Requirements
- 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
Compensation: $87,200 - $182,000 base
Vacancy posted a month ago
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