Details:

  • Compensation: $22 - $28/hour
  • Benefits: Medical, Dental, Vision
  • Employment Classification: Direct Hire
  • Status: On-Site
  • Job ID: 21169

Job Title: Clinical Research Coordinator

Work Location: Lauderdale County, Tennessee

Summary:

This position offers an opportunity to play a key role in the management and oversight of clinical trials within a supportive and mission-driven environment. The Clinical Research Coordinator is responsible for ensuring the smooth operation of research studies, maintaining compliance with regulatory standards, and supporting participant safety and data integrity. The role requires strong attention to detail, proficiency in medical terminology, and hands-on experience with clinical research processes, including phlebotomy.

Responsibilities:

  • Coordinate daily activities of clinical trials, ensuring strict adherence to study protocols and established timelines.
  • Collect, analyze, and accurately document trial data to support compliance and reporting requirements.
  • Perform and oversee blood sampling procedures, ensuring proper handling and meticulous documentation.
  • Participate in training on clinical trial protocols and operational procedures.
  • Work collaboratively with healthcare professionals to uphold participant safety and maintain data integrity.
  • Utilize specialized software for efficient data capture, management, and reporting.
  • Apply knowledge of medical terminology to facilitate effective communication with team members and stakeholders.
  • Ensure all research activities comply with ethical standards and regulatory guidelines throughout the study lifecycle.

Qualifications:

  • At least one year of experience coordinating clinical research projects from initiation to completion.
  • Minimum of two years’ experience in clinical trials coordination preferred.
  • Proficiency in data entry and management systems.
  • Demonstrated knowledge of medical terminology relevant to clinical research.
  • Phlebotomy skills and experience with blood sampling techniques required.
  • Experience with patient recruitment for clinical studies required.
  • Excellent organizational skills, attention to detail, and ability to manage multiple tasks simultaneously.
  • Clinical experience preferred but not required.

Published Category: Clinical Operations & Development

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