Clinical Research Coordinator III- School of Medicine, Obstetrics and Gynecology Oncology
This is a full-remote position available in Georgia, Indiana, and Oregon (USA).
About the Role
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.
This position supports clinical research, and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher. While tasks are generally required to be performed in-person at an Emory University location, remote work-from-home 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 (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, specimen collection, or diagnostics.
- May perform some supervisory duties.
- Performs related approved responsibilities as required.
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 of 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.