Clinical Research Coordinator I - School of Medicine Psychiatry (PREVENT Study)

Emory•Atlanta, GA

1d•Hybrid

About The Position

The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials. This individual will work with Drs van Rooij and Stevens on the NIH funded PREVENT Clinical trial. The ideal candidate has clinical research experience, MRI experience, and an enthusiasm for neuromodulation and its treatment of Post-Traumatic Stress Disorder.

Requirements

High School Diploma or GED and three years of administrative support experience.
Two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.
Clinical research experience.
MRI experience.

Nice To Haves

Enthusiasm for neuromodulation and its treatment of Post-Traumatic Stress Disorder.

Responsibilities

Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Assists with patient recruitment.
Attends study meetings.
Orders and maintains equipment and supplies.
Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
Assists with quality assurance and tracks regulatory submissions.
Performs related approved responsibilities as required.