Clinical Research Coordinator IV

Emory University

Clinical Research Coordinator conducting and overseeing clinical trials at Emory University. Managing projects, training, and compliance for research administration activities in a medical setting.

Posted 7/2/2026full-timeAtlanta • 🇺🇸 United StatesSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research projects, including recruitment and retention strategies for participants, compliance with study protocols, and budget monitoring. Proficient in developing grant proposals and leading research administration teams to ensure operational excellence.

Highest-signal resume keywords

Clinical Research ManagementGrant Proposal DevelopmentCompliance AuditingParticipant Recruitment StrategiesLeadership in Research Administration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trials ManagementBudget MonitoringStudy Protocol ImplementationResearch AdministrationData AnalysisRegulatory ComplianceProject ManagementAudit ProceduresResearch Participant RetentionClinical Research Experience

Soft Skills

LeadershipCommunicationTeam SupervisionProblem SolvingEducation and Training

Tools & Technologies

Clinical Research Information SystemsLaboratory ProceduresStudy-Related Equipment Management

Certifications & Qualifications

Certified Research Administrator (CRA)Clinical Research Coordinator (CRC)Licensed Practical Nurse (LPN)

Industry Keywords

Clinical TrialsResearch GrantsStudy ProtocolsExpenditure MonitoringResearch Compliance

About the role

Key responsibilities & impact

Recruits, orients, and supervises research administration staff or independently manages the most complex research administration activities associated with the conduct of clinical trials
Manages a large or multiple smaller clinical research projects
Manages clinical trials related information systems
Supervises the implementation of and adherence to study protocols
Monitors expenditures and adherence to study budgets and resolves CAS issues
Educates research staff on established policies, processes and procedures
Determines effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials
Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes
Plans, identifies, and handles study-related equipment and facilities needs
Provides leadership and expertise in identifying and completing research grants, study materials, brochures and correspondence
Develops and submits grant proposals
Leads or chairs committees or task forces to address and resolve significant issues
Performs related approved responsibilities as required

Requirements

What you’ll need

High School Diploma or GED and nine years of clinical research experience
Two years of college in a scientific, health-related, or business administration program and seven years clinical research experience
Licensed as a Practical Nurse (LPN) and six years clinical research experience
Bachelor's degree in a scientific, health-related, or business administration program and five years of clinical research experience
Master's degree, MD or PhD in a scientific, health-related, or business administration program and two years of clinical research experience
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred

Benefits

Comp & perks

Health and Safety Information
Flexible work arrangements