Full-Time

Clinical Research Coordinator 3

The Hope Clinic

Posted on 10/3/2025

Deadline 10/7/26
Emory University

Emory University

No salary listed

Decatur, GA, USA

Hybrid

This role requires residency in the state of GA and allows for regular work from home with a flexible weekly schedule based on business needs.

Category
Medical, Clinical & Veterinary (1)
Biology & Biotech (2)
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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.
  • Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
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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Total Funding

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INACTIVE