Clinical Research Associate, Early Clinical Development
$90.2k - $175.1kIQVIA
Clinical Research Associate position supporting Phase I early clinical development trials across multiple US locations. The role involves conducting site visits, monitoring protocol compliance, managing enrollment, and ensuring data integrity while working with cross-functional teams.
Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits aligned with GCP and ICH guidelines
- Collaborate with site staff to implement recruitment strategies and track enrollment progress
- Provide protocol training to site personnel and maintain ongoing communication
- Assess site performance and escalate compliance or data quality issues
- Maintain essential trial documentation in Trial Master File and Investigator Site File systems
Requirements
- Bachelor's degree in life sciences or health-related field or equivalent experience
- Minimum 1.5 years of on-site clinical trial monitoring experience
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements
- Ability to travel as required by assigned projects
- Experience with site management documentation and regulatory files
Compensation: $90,200-$175,100 base
$90.2k - $175.1k
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