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

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