Clinical Research Coordinator II

Updated: 4 days ago

Job Description


  • Handles administrative activities generally associated with the conduct of clinical trials.
  • Provides guidance to less experienced staff.
  • Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.
  • 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.


(1.) High School Diploma or GED


5 years of clinical research experience. OR

(2.) 2 years of college in a scientific, health related, or business administration program


3 years clinical research experience OR

(3.) Licensed as a practical nurse (LPN)


2 years clinical research experience OR

(4.) Bachelor's degree in a scientific, health related, or business administration related program


1 year of clinical research experience OR

(5.) 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.

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