Clinical Research Coordinator I - School of Medicine Psychiatry

Emory • Atlanta, GA

12h • Hybrid

About The Position

This new clinical research coordinator position will be part of the Clinical and Research Programs for Psychosis (CRPP) at Grady Health System. The CRPP is an interdisciplinary collaboration between Emory and Grady that provides evidence-based, clinical care and offers cutting-edge research opportunities for individuals with serious mental illness across the metro Atlanta area. Our clinical services specialize in clozapine and early psychosis. The new clinical research coordinator will work on various research projects in our overall program, but have a particular focus towards our new clinical high risk for psychosis program serving youth and young adults aged 14-25. The program is headquartered at Grady Behavioral Health Clinic at 10 Park Place, under the Adult Outpatient Clinic. The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.

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.
• A Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.
• 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

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level