Clinical Research Coordinator II - School of Medicine, Thoracic Surgery
Emory•Atlanta, GA
•Hybrid
About The Position
The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials. This position supports clinical research and requires clinical training requirements to be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher. Tasks are generally performed in person at two Emory locations, EUHM and ESJH, during an introductory period, with remote flexibility for eight hours per week after that period.
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 credentialing category of Clinical Researcher.
Responsibilities
- Manage research project databases, develop flow sheets and other study-related documents, and complete source documents and case report forms.
- Provide guidance to less experienced staff.
- Interface with research participants, determine eligibility, and consent participants according to protocol.
- Approve orders for supplies and equipment maintenance.
- Assist in developing recruitment strategies and conduct participant screenings, including interviews and questionnaires.
- Supervise the collection and processing of study specimens.
- Establish case packages for study procedures, monitor procedure scheduling and charges, and coordinate other services as needed.
- Ensure compliance with research protocols, review case report forms, audit them for accuracy against source documents, and attend sponsor monitoring meetings.
- Prepare regulatory submissions.
- Perform phlebotomy or diagnostics when appropriately credentialed and trained.
- Perform related approved responsibilities as required.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
