Clinical Research Coordinator III - School of Medicine Anesthesiology

Emory•Atlanta, GA

13d•Onsite

About The Position

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. Description KEY 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. Employees in this classification may be required to work with, take specific precautions against and/or be immunized against potentially hazardous agents. Transports and processes biological specimens (training provided). May perform some supervisory duties. Performs emergency CPR. 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 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
Must have transportation and be able to work at Emory University Hospital (primary site) and/or Emory University Hospital Midtown.
NOTE: Position tasks are required to be performed in-person at an Emory University location; working remote is not an option. Emory reserves the right to change this status with notice to employee.

Nice To Haves

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.

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.
Employees in this classification may be required to work with, take specific precautions against and/or be immunized against potentially hazardous agents.
Transports and processes biological specimens (training provided).
May perform some supervisory duties.
Performs emergency CPR.
Performs related approved responsibilities as required.