About The Position

The Clinical Research Coordinator handles or assists with administrative activities associated with conducting clinical trials. The role supports clinical research and requires clinical training requirements to be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher. The position offers regular work-from-home opportunities, but the employee must be able to commute to Emory University on a flexible weekly schedule based on business needs and departmental guidelines. Residency in Georgia is required. Emory reserves the right to change remote-work status with notice.

Requirements

  • High school diploma or GED and three years of administrative support experience; or two years of college in a scientific, health-related, or business administration program and one year of administrative support or customer service experience; or an LPN license and one year of administrative support or licensed practical nursing experience; or a bachelor's degree, master's degree, MD, or PhD in a scientific, health-related, or business administration program.
  • Clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.
  • Must reside in Georgia.
  • Must be able to commute to Emory University on a flexible weekly schedule based on business needs.

Responsibilities

  • Maintain data pertaining to research projects, complete source documents and case report forms, and perform data entry.
  • Assist with patient recruitment.
  • Attend study meetings.
  • Order and maintain equipment and supplies.
  • Review medical records and/or conduct screenings to recruit study participants; perform interviews and quality-of-life questionnaires.
  • Collect study specimens according to protocol, which may include phlebotomy, processing, and preparation for shipping.
  • Coordinate services, schedule procedures, create and maintain case packages, and monitor charges.
  • Assist with quality assurance and track regulatory submissions.
  • Perform related approved responsibilities as required.
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