Full-Time

Clinical Research Coordinator 3

School of Medicine, Surgery

Posted on 9/19/2025

Deadline 1/20/27
Emory University

Emory University

No salary listed

Atlanta, GA, USA

Hybrid

Hybrid work: in-person at Emory; remote days may be granted at department discretion.

Category
Medical, Clinical & Veterinary (1)
Required Skills
Ruby
Requirements
  • High School Diploma or GED and seven years of clinical research experience.
  • Or two years of college in a scientific, health related or business administration program and five years of clinical research experience
  • Or licensed as a Practical Nurse (LPN) and four years of clinical research experience
  • Or bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
  • Or master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
  • Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
  • 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.
  • Employee must participate in a 24/7 on-call rotation with other team members to enroll eligible transplant recipients.
  • 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.
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 serious adverse events; 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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