Clinical Research Coordinator - General Interest

Headlandsresearch

Rolling Hills Estates, California, US
On-site
Clinical trial coordination
Gcp/ich guidelines
Edc data entry
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities

Job Summary

  • At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities.
  • Coordinate all aspects of assigned clinical trials from site initiation through close-out.
  • This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision.

Matching Summary

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities.

Skills & Requirements

Must-have

  • Clinical trial coordination
  • GCP/ICH guidelines
  • EDC data entry
  • Subject recruitment
  • Informed consent

Nice-to-have

  • Work-life balance
  • Team-based approach
  • Meaningful work

Key Requirements

  • At least one year of experience coordinating Phase 2–4 industry-sponsored clinical trials required
  • Bachelor's Degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP

Work Rights

Not specified

Tailored Resume

Cover Letter