Clinical Research Coordinator III – Dermatology

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 11/10/2026full-timeAtlanta • Georgia • United StatesSeniorLeadWebsite

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 phlebotomy and clinical research operations, with strong organizational skills to handle multiple projects effectively.

Highest-signal resume keywords

Clinical Research ExperienceRegulatory/IRB SubmissionsPhlebotomyCertified Research Administrator (CRA)Clinical Research Coordinator (CRC)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ManagementStudy Start-Up ActivitiesContractingBilling and InvoicingInventory ManagementRecords RetentionBiospecimen CollectionProcessing and HandlingStudy CloseoutGrant Proposal Development

Soft Skills

Organizational SkillsLeadershipTraining and Guidance

Certifications & Qualifications

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

Industry Keywords

Clinical TrialsResearch ProtocolsParticipant RecruitmentCompliance AuditsSAE ReportingEmory Healthcare 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 research participants and retaining participants in long-term clinical trials
Periodically audit operations, including laboratory procedures, to ensure compliance with applicable regulations
Provide leadership in identifying and implementing corrective actions and processes
Monitor IRB submissions and respond to requests and questions
Interface with study sponsors and monitors, report SAEs, and resolve study queries
Provide leadership in determining, recommending, and implementing improvements to policies and processes
Assist in developing grant proposals and protocols
With appropriate credentialing and training, perform phlebotomy, specimen collection, or diagnostics
May perform some 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
Experience with the administrative and operational aspects of clinical research and clinical trials, including regulatory/IRB submissions, study start-up activities, contracting, billing and invoicing, inventory management, study closeout, and records retention/maintenance
Experience with phlebotomy biospecimen collection, processing, handling, storage, and shipment in support of clinical research studies
Strong organizational skills with the ability to manage multiple studies, priorities, and deadlines simultaneously
All 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
Reasonable accommodations for qualified individuals with disabilities upon request