Clinical Research Coordinator (CRC)

Site Ops Participants Data GCP Compliance
Site Ops Participants Data GCP Compliance

Career Opportunity

Coordinate day-to-day clinical operations

The CRC manages onsite trial activities—participant recruitment, visit scheduling, data capture, and protocol adherence—ensuring quality at the site level.

Role Summary

You will run daily site operations, coordinate with investigators and CRAs, and maintain accurate documentation and source data.

Key Responsibilities

  • Screen and enroll participants; obtain informed consent properly.
  • Schedule visits; manage supplies, IP accountability, and sample logistics.
  • Collect source data and ensure timely, accurate eCRF entry.
  • Maintain protocol/GCP compliance and readiness for monitoring/audits.
  • Coordinate communications between site, sponsor/CRO, and CRAs.

Qualifications

  • Bachelor’s degree (life science/health preferred) with strong organization and communication skills.
  • Prior site coordination experience is preferred.

Technical Skills

  • Familiarity with EDC/eCRF systems; accurate source documentation.
  • Basic understanding of ICH-GCP and site SOPs.

Soft Skills

  • People-centric, detail-oriented, and highly organized.
  • Clear communication with investigators and patients.
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Position Details

  • Location: Site-based
  • Department: Clinical Operations
  • Type: Full-Time
  • Experience: 1–3 years
  • Reports To: Principal Investigator / Site Manager

Nice to Have

  • Phlebotomy or sample processing experience.
  • Patient-facing experience in hospital or trial settings.

Frequently Asked Questions

Clinical Site Operations

A quick look at site coordination best practices.

Primarily EDC/eCRF, lab portals, and site SOP templates for documentation and logistics.

Yes—participant engagement and visit coordination are core parts of the role.

Yes—structured onboarding with SOPs, job shadowing, and regular check-ins with the site lead.