Full-Time

Clinical Research Coordinator 2

School of Medicine Neurobehavior

Posted on 9/28/2025

Deadline 2/26/27
Emory University

Emory University

No salary listed

Atlanta, GA, USA

Hybrid

GA residency required; remote work allowed regularly with commuting to Emory on a flexible weekly schedule.

Category
Medical, Clinical & Veterinary (2)
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Requirements
  • High School Diploma or GED and five years of clinical research experience.
  • Or two years of college in a scientific, health related, or business administration program and three years clinical research experience.
  • Or a license as a practical nurse (LPN) and two years clinical research experience.
  • Or a Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience.
  • Or a Master's degree, MD or PhD in a scientific, health related or business administration program.
  • This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.
  • Residency in the state of GA is required; remote work is allowed with commute to Emory University on a flexible weekly schedule; schedule is based on department guidelines; Emory reserves the right to change remote work status with notice to employee.
Responsibilities
  • Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.
  • Provides guidance to less experienced staff.
  • Interfaces with research participants, determines eligibility and consents study participants according to protocol.
  • Approves orders for supplies and equipment maintenance.
  • Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires.
  • Supervises collection of study specimens and processing.
  • Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed.
  • Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors.
  • Prepares regulatory submissions.
  • With appropriate credentialing and training may perform phlebotomy or diagnostics.
  • Performs related approved responsibilities as required.

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