Clinical Research Coordinator II - School of Medicine, Endocrinology

Emory University•Atlanta, GA

4h•Onsite

About The Position

The Clinical Research Coordinator II handles administrative activities generally associated with conducting clinical trials. The role supports clinical research and requires clinical training requirements to be tracked and monitored through Emory Healthcare under the Clinical Researcher credentialing category. The position involves working in an inpatient hospital setting across multiple locations (EUH, EUHM, and Grady), with flexibility for occasional evening and weekend coverage.

Requirements

High school diploma or GED and five years of clinical research experience; or two years of college in a scientific, health-related, or business administration program and three years of clinical research experience; or practical nurse (LPN) licensure and two years of clinical research experience; or a bachelor's degree in a scientific, health-related, or business administration-related program and one year of clinical research experience; or a master's degree, MD, or PhD in a scientific, health-related, or business administration program.
Clinical training requirements must be tracked and monitored through Emory Healthcare under the Clinical Researcher credentialing category.
Comfort working in an inpatient hospital setting across multiple locations (EUH, EUHM, and Grady).
Flexibility for occasional evening and weekend coverage.

Responsibilities

Manages research project databases, develops flow sheets and other study-related documents, and completes source documents and case report forms.
Provides guidance to less experienced staff.
Interfaces with research participants, determines eligibility, and obtains informed consent according to protocol.
Approves orders for supplies and equipment maintenance.
Assists in developing recruitment strategies and conducting participant screenings, including interviews and questionnaires.
Supervises collection and processing of study specimens.
Establishes case packages for study procedures, monitors procedure scheduling and charges, and coordinates other services as needed.
Ensures compliance with research protocols, reviews case report forms, audits them for accuracy against source documents, and attends sponsor monitoring meetings.
Prepares regulatory submissions.
May perform phlebotomy or diagnostics with appropriate credentialing and training.
Performs related approved responsibilities as required.