Senior Clinical Research Associate, Early Clinical Development
$87.2k - $169.3kIQVIA
IQVIA is seeking a Senior Clinical Research Associate for early-stage clinical development based on the East Coast. The role involves managing clinical trial sites, ensuring protocol compliance, and maintaining data integrity across Phase 1 and other trial phases.
Responsibilities
- Conduct site visits including selection, initiation, monitoring, and closeout activities
- Collaborate with site staff to implement recruitment strategies and track enrollment progress
- Provide protocol training to site personnel and maintain ongoing communication
- Monitor protocol compliance, data quality, and regulatory submission status
- Maintain essential documents in Trial Master Files and Investigator Site Files per regulatory standards
Requirements
- Bachelor's degree in life sciences or health-related field
- 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 project assignments
Compensation: $87,200–$169,300 base
$87.2k - $169.3k
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