Hybrid Senior Clinical Research Associate, Early Clinical Development

Posted last week

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About the role

  • Clinical Research Associate responsible for monitoring compliance with clinical trial protocols at IQVIA. Collaborating with site staff and ensuring data integrity in clinical research operations.

Responsibilities

  • Monitor and manage clinical sites for compliance with study protocols
  • Conduct site visits including selection, initiation, monitoring, and close-out
  • Collaborate with site staff for subject recruitment strategies
  • Deliver training to site personnel
  • Assess site performance and monitor study progress
  • Ensure collection and maintenance of essential documents

Requirements

  • Bachelor’s degree in life sciences or health-related field (or equivalent experience)
  • At least 1.5 years of on-site monitoring experience
  • Strong understanding of GCP, ICH guidelines, and regulatory requirements
  • Ability to travel as required by the project

Benefits

  • Health insurance
  • 401(k) matching
  • Paid time off
  • Flexible work arrangements
  • Professional development opportunities
  • Bonuses

Job title

Senior Clinical Research Associate, Early Clinical Development

Job type

Experience level

Senior

Salary

$87,200 - $169,300 per year

Degree requirement

Bachelor's Degree

Location requirements

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