Full-Time

Clinical Research Coordinator 3

Department of Gynecology and Obstetrics

Posted on 10/3/2025

Deadline 10/8/25
Emory University

Emory University

No salary listed

Atlanta, GA, USA

Hybrid

Position tasks are generally required to be performed in-person at an Emory University location. Remote work from home day options may be granted at department discretion.

Category
Medical, Clinical & Veterinary (1)
Requirements
  • High School Diploma or GED and seven years of clinical research experience
  • Two years of college in a scientific, health related or business administration program and five years of clinical research experience
  • Licensed as a Practical Nurse (LPN) and four years of clinical research experience
  • Bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
  • Master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
Responsibilities
  • Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects
  • Trains and provides guidance to less experienced staff
  • Oversees data management for research projects
  • Interfaces with research participants and resolves issues related to study protocols
  • Authorizes purchases for supplies and equipment maintenance
  • Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials
  • Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes
  • Monitors IRB submissions and responds to requests and questions
  • Interfaces with study sponsors, monitors and reports SAEs; resolves study queries
  • Provides leadership in determining, recommending, and implementing improvements to policies/processes
  • Assists in developing grant proposals and protocols
  • With appropriate credentialing and training may perform phlebotomy, specimens collection or diagnostics
  • May perform some supervisory duties
  • Performs related approved responsibilities as required
Desired Qualifications
  • Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred

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