Clinical Research Coordinator I Or Ii

Headlands Research

Portland, OR, US
On-site
Phase 2-4 industry-sponsored clinical trial experience
Fda regulations and ich-gcp knowledge
Edc data entry and query resolution skills
The role involves coordinating all aspects of assigned clinical trials from site initiation through close-out while ensuring strict compliance with FDA regulations and GCP guidelines

Job Summary

  • The role involves coordinating all aspects of assigned clinical trials from site initiation through close-out while ensuring strict compliance with FDA regulations and GCP guidelines.
  • Candidates will collaborate with seasoned investigators and clinical staff on complex, meaningful studies rather than high-volume turnover environments.
  • The position offers stability within a growing research network that values strong operations, clear SOPs, and a team-based approach to clinical research.

Matching Summary

The role involves coordinating all aspects of assigned clinical trials from site initiation through close-out while ensuring strict compliance with FDA regulations and GCP guidelines.

Skills & Requirements

Must-have

  • Phase 2-4 industry-sponsored clinical trial experience
  • FDA regulations and ICH-GCP knowledge
  • EDC data entry and query resolution skills
  • Onsite work in Portland OR required
  • Subject recruitment and informed consent management

Nice-to-have

  • Experience with memory studies and psychiatric conditions
  • Strong multidisciplinary collaboration skills
  • Ability to own studies with precision
  • Phlebotomy and ECG procedure training
  • Commitment to work-life balance

Key Requirements

  • At least two years managing multiple Phase 2-4 studies as primary coordinator
  • Bachelor's degree or 2 years college in health-related program
  • Knowledge of ICH GCP and clinical trial operations
  • Proficiency with EDC, IVRS, and clinical research platforms

Work Rights

Not specified

Tailored Resume

Cover Letter