Clinical Research Coordinator

Headlandsresearch

Lake Worth, FL, United States
On-site
Fda regulations
Gcp/ich guidelines
Sponsor protocols
Coordinate all aspects of assigned clinical trials from site initiation to study close-out

Job Summary

  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out.
  • Manage subject recruitment, informed consent, and retention strategies.
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders.

Matching Summary

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

Skills & Requirements

Must-have

  • FDA regulations
  • GCP/ICH guidelines
  • sponsor protocols
  • ALCOA-C standards
  • EDC query resolution
  • adverse event reporting
  • monitoring visits
  • regulatory documentation

Nice-to-have

  • fast-paced environment
  • patient-centered care
  • mission-driven culture
  • advancing medicine
  • improving patient outcomes

Key Requirements

  • Minimum of 1 year of experience as a Clinical Research Coordinator
  • Minimum of 2 years of experience as a Research Assistant in Clinical Research
  • High school diploma or GED
  • Bilingual (English/Spanish) is strongly preferred

Work Rights

Not specified

Tailored Resume

Cover Letter