Job Description
Experience Required: 2+ years at a private research site
Overview:
We are seeking an experienced Clinical Research Coordinator to support the day-to-day execution of clinical trials at a private research site. The CRC will work closely with investigators, sponsors, and CROs to ensure studies are conducted in compliance with GCP, protocol requirements, and regulatory standards.
Key Responsibilities:
- Coordinate and manage clinical trial activities from study start-up through close-out
- Screen, enroll, and consent study participants
- Conduct study visits and maintain accurate source documentation
- Ensure compliance with protocols, GCP, and regulatory requirements
- Manage regulatory binders, IRB submissions, and study documentation
- Communicate with sponsors, CROs, and monitors
- Support data entry and query resolution in EDC systems
Qualifications:
- Minimum 2 years of CRC experience at a private research site
- Strong knowledge of GCP and clinical trial workflows
- Experience with subject-facing visits and protocol execution
- Excellent organizational and communication skills
- Ability to manage multiple studies simultaneously
Compensation & Employment Type:
- $31/hour (1099 contractor) - 25-40/hrs a week
- Potential for conversion to W-2 based on performance and site needs
Job Tags
For contractors,