Clinical Research Coordinator IV- School of Medicine, Emergency Medicine

Emory University•Atlanta, GA

2d•Onsite

About The Position

The Emory Critical Illness Center is looking for a Clinical Research Coordinator IV to assist in supporting its critical care and emergency medicine research. Clinical research experience in: participant screening, recruitment, CRF completion, data entry and regulatory activities as it relates to day-to-day study management is preferred. This will be an in-person full-time position with on-call work requirements.

Requirements

High School Diploma or GED and nine years of clinical research experience.
Two years of college in a scientific, health related, or business administration program and seven years clinical research experience
Licensed as a Practical Nurse (LPN) and six years clinical research experience
Bachelor's degree in a scientific, health related or business administration program and five years of clinical research experience
Master's degree, MD or PhD in a scientific, health related, or business administration program and two years of clinical research experience
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.

Nice To Haves

Clinical research experience in: participant screening, recruitment, CRF completion, data entry and regulatory activities as it relates to day-to-day study management is preferred.
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.

Responsibilities

Recruits, orients, and supervises research administration staff or independently manages the most complex research administration activities associated with the conduct of clinical trials.
Manages a large or multiple smaller clinical research projects.
Manages clinical trials related information systems.
Supervises the implementation of and adherence to study protocols.
Monitors expenditures and adherence to study budgets and resolves CAS issues.
Educates research staff on established policies, processes and procedures.
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.
Plans, identifies, and handles study related equipment and facilities needs.
Provides leadership and expertise in identifying and completing research grants, study materials, brochures and correspondence.
Develops and submits grant proposals.
Leads or chairs committees or task forces to address and resolve significant issues.
Performs related approved responsibilities as required.