Clinical Research Associate, Early Clinical Development

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