Temporary Clinical Research Coordinator I, Ii, Or Iii

Headlandsresearch

Rolling Hills Estates, California, US
$75,000 py
On-site
Coordinate clinical trials
Conduct subject visits
Maintain compliance with protocols
Coordinate all aspects of assigned clinical trials from site initiation through close-out

Job Summary

  • Coordinate all aspects of assigned clinical trials from site initiation through close-out.
  • Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs.
  • Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained).

Matching Summary

Coordinate all aspects of assigned clinical trials from site initiation through close-out.

Salary

$75,000

Skills & Requirements

Must-have

  • Coordinate clinical trials
  • Conduct subject visits
  • Maintain compliance with protocols
  • Manage subject recruitment
  • Ensure timely EDC data entry
  • Report AEs and deviations
  • Collaborate with investigators and sponsors

Nice-to-have

  • Meaningful work
  • Work-life balance
  • Team-based approach
  • Data quality
  • Patient experience

Key Requirements

  • At least one year of experience coordinating Phase 2–4 industry-sponsored clinical trials
  • High school diploma or GED required; Bachelor’s degree preferred
  • Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations

Work Rights

Not specified

Tailored Resume

Cover Letter