Clinical Research Coordinator II

Emory University

Clinical Research Coordinator II at Hope Clinic handling administrative tasks for infectious diseases clinical trials. Supervising participant engagement and ensuring protocol compliance in clinical research.

Posted 7/2/2026full-timeDecatur • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, ensuring compliance with research protocols, and guiding less experienced staff. Proficient in developing recruitment strategies, preparing regulatory submissions, and performing clinical research activities.

Highest-signal resume keywords

Clinical Research ExperienceRegulatory SubmissionsPhlebotomyResearch Protocol ComplianceStaff Supervision

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementData ManagementSource Document ReviewCase Report Form CompletionSpecimen CollectionInterviewing TechniquesRecruitment Strategy DevelopmentFlow Sheet DevelopmentEligibility DeterminationDiagnostic Procedures

Soft Skills

GuidanceCommunicationCollaborationProblem-SolvingLeadership

Certifications & Qualifications

Licensed Practical Nurse (LPN)

Industry Keywords

Clinical TrialsResearch ProtocolsParticipant ConsentStudy ProceduresMonitoring Meetings

About the role

Key responsibilities & impact

Handles administrative activities generally associated with the conduct of clinical trials.
Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.
Provides guidance to less experienced staff.
Interfaces with research participants, determines eligibility and consents study participants according to protocol.
Approves orders for supplies and equipment maintenance.
Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires.
Supervises collection of study specimens and processing.
Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed.
Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors.
Prepares regulatory submissions.
With appropriate credentialing and training may perform phlebotomy or diagnostics.
Performs 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 clinical research experience.
Or a licensed as a practical nurse (LPN) and two years 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.

Benefits

Comp & perks

Health and Safety Information Not Applicable