Clinical Research Coordinator III

Emory University

. Independently manage significant and key aspects of a large clinical trial or all aspects of one or more small trials or research projects .

Posted 9/21/2026full-timeAtlanta • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, including oversight of data management, regulatory compliance, and participant recruitment. Proficient in clinical procedures such as phlebotomy and specimen collection, with a strong focus on training and mentoring staff.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory Compliance AuditingParticipant Recruitment StrategiesPhlebotomy and Specimen CollectionCertified Research Administrator (CRA)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ExperienceData ManagementGrant Proposal DevelopmentIRB Submission MonitoringCorrective Action Implementation

Soft Skills

Training and MentoringProblem ResolutionLeadership

Certifications & Qualifications

Certified Research Administrator (CRA)Clinical Research Coordinator (CRC)

Industry Keywords

Clinical TrialsResearch ProtocolsAdverse Event ReportingHuman Subjects ResearchClinical Researcher Credentialing

About the role

Key responsibilities & impact

Independently manage significant and key aspects of a large clinical trial or all aspects of one or more small trials or research projects
Train and provide guidance to less experienced staff
Oversee data management for research projects
Interface with research participants and resolve issues related to study protocols
Authorize purchases for supplies and equipment maintenance
Develop strategies for promoting and recruiting research participants and retaining participants in long-term clinical trials
Audit operations, including laboratory procedures, for regulatory compliance
Identify and implement corrective actions and processes
Monitor IRB submissions and respond to requests and questions
Interface with study sponsors and monitors
Report serious adverse events (SAEs) and resolve study queries
Lead improvements to policies and processes
Assist in developing grant proposals and protocols
Perform phlebotomy, specimen collection, or diagnostics with appropriate credentialing and training
May perform supervisory duties
Perform related approved responsibilities as required

Requirements

What you’ll need

High School Diploma or GED and seven years of clinical research experience
Or two years of college in a scientific, health related or business administration program and five years of clinical research experience
Or licensed as a Practical Nurse (LPN) and four years of clinical research experience
Or bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
Or master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
Clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher
Position involves clinical patient contact and working with human blood, body fluids, tissues, or other potentially infectious materials

Benefits

Comp & perks

Equal opportunity employment
Reasonable accommodations for qualified individuals with disabilities
Access to university programs and facilities without discrimination