Clinical Research Coordinator Job at CRO Strategies, Knoxville, TN

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  • CRO Strategies
  • Knoxville, TN

Job Description

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,

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