Clinical Research Coordinator II- School of Medicine, Rheumatology

Emory•Atlanta, GA

1d•Onsite

About The Position

The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials. The role supports clinical research and requires all clinical training requirements to be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher. Position tasks must be performed in person at an Emory University location; remote work is not an option. Emory reserves the right to change this status with notice to the employee.

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 nursing licensure (LPN) 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 credentialing category of Clinical Researcher.
Position tasks must be performed in person at an Emory University location; remote work is not an option.

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 consents study participants according to protocol.
Approves orders for supplies and equipment maintenance.
Assists in developing recruitment strategies and conducts 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, and audits them for accuracy against source documents.
Attends monitoring meetings with sponsors.
Prepares regulatory submissions.
May perform phlebotomy or diagnostics with appropriate credentialing and training.
Performs related approved responsibilities as required.