Clinical Research Coordinator III – Biomedical Engineering

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 11/2/2026full-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 training staff and implementing process improvements while ensuring adherence to study protocols.

Highest-signal resume keywords

Clinical Trial ManagementData ManagementRegulatory ComplianceParticipant RecruitmentClinical Research Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PhlebotomySpecimen CollectionDiagnosticsGrant Proposal DevelopmentPolicy Implementation

Soft Skills

Training and GuidanceProblem ResolutionLeadership

Certifications & Qualifications

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

Industry Keywords

IRB SubmissionsSAE MonitoringClinical ResearchLaboratory ProceduresClinical 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
Determine effective strategies for promoting, recruiting, and retaining research participants in long-term clinical trials
Periodically audit operations, including laboratory procedures, for regulatory compliance
Lead identification and implementation of corrective actions and processes
Monitor IRB submissions and respond to requests and questions
Interface with study sponsors, monitor and report SAEs, and resolve study queries
Lead determination, recommendation, and implementation of policy and process improvements
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

Benefits

Comp & perks

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