Clinical Research Coordinator II

Emory University

Clinical Research Coordinator II managing clinical trials at Emory University’s Winship Cancer Institute. Coordinating participants, specimens, regulatory submissions, databases, and protocol compliance.

Posted 8/12/2026full-timeAtlanta • 🇺🇸 United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research projects, ensuring compliance with protocols, and conducting participant interactions. Proficient in data management, regulatory submissions, and clinical training oversight.

Highest-signal resume keywords

Clinical Research ExperienceRegulatory SubmissionsPhlebotomyParticipant ScreeningCompliance Monitoring

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ManagementFlow Sheet DevelopmentSource Document ReviewCase Report Form CompletionSpecimen CollectionStudy Procedure CoordinationRecruitment Strategy DevelopmentClinical Training MonitoringDiagnostic ProceduresClinical Protocol Compliance

Soft Skills

Guidance to StaffInterpersonal CommunicationSupervisionProblem SolvingTeam Collaboration

Certifications & Qualifications

LPN LicenseClinical Researcher Credentialing

Industry Keywords

Clinical ResearchHuman Subjects ResearchInfectious Materials HandlingResearch ProtocolsParticipant Consent

About the role

Key responsibilities & impact

Manage research project databases, develop flow sheets and study-related documents, and complete source documents/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, interviews, and questionnaires
Supervise collection and processing of study specimens
Establish case packages for study procedures, monitor procedure scheduling and charges, and coordinate other services
Ensure compliance with research protocols
Review case report forms and audit accuracy against source documents
Attend sponsor monitoring meetings
Prepare regulatory submissions
Perform phlebotomy or diagnostics when appropriately credentialed and trained
Perform related approved responsibilities as required

Requirements

What you’ll need

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 an LPN license 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
Position involves clinical patient contact
Must work with human blood, body fluids, tissues, or other potentially infectious materials

Benefits

Comp & perks

Remote work from home day options may be granted at department discretion
Equal opportunity employer
Reasonable accommodations for qualified individuals with disabilities