IQVIA

Clinical Research Associate, Sponsor Dedicated

IQVIA

full-time

Posted on:

Location Type: Hybrid

Location: CaliforniaKansasUnited States

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Salary

💰 $64,000 - $189,000 per year

About the role

  • Perform monitoring and site management work to ensure sites conduct study(ies) as required
  • Perform site monitoring visits in accordance with Good Clinical Practice and regulatory requirements
  • Manage progress of assigned studies by tracking regulatory submissions and approvals
  • Collaborate and liaise with study team members for project execution support

Requirements

  • 2.5 years of clinical research coordination experience at site level
  • Nursing or University Degree (US Bachelor Level or equivalent) in one of the life sciences
  • Knowledge of electronic data capture preferred
Benefits
  • Health insurance
  • Retirement plans
  • Paid time off
  • Flexible work arrangements
  • Professional development opportunities
  • Bonuses
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical research coordinationsite managementregulatory submissionsGood Clinical Practiceelectronic data capture
Soft Skills
collaborationliaisonproject execution support