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Senior Clinical Research Associate, Early Clinical Development

$87.2k - $169.3k

IQVIA

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

Vacancy posted a month ago
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