Clinical Research Coordinator

Duke Careers

. Obtain informed consent from patients using paper consent forms and REDCap e-consent platforms .

Posted 9/17/2026full-timeDurham • North Carolina • United StatesJuniorMid-Level💰 $61,026 - $101,959 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in obtaining informed consent, coordinating tissue samples, and ensuring compliance with regulatory standards. Proficient in utilizing patient health data and reviewing IRB-approved protocols to support research activities.

Highest-signal resume keywords

Informed Consent AcquisitionRegulatory CompliancePatient Health Data UtilizationIRB Protocol ReviewBiospecimen Collection

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Research ExperienceTissue Sample CoordinationData ExtractionAbstract GenerationQuality Control Standards Compliance

Soft Skills

CollaborationOrganizational SkillsCommunication SkillsGoal SettingProactive Communication

Tools & Technologies

REDCap E-Consent PlatformDuke Electronic Medical RecordDuke Clinical Laboratories Systems

Certifications & Qualifications

Associate's DegreeBachelor's Degree (Substitution for Experience)College of American Pathologists (CAP) Guidelines Compliance

Industry Keywords

IRB-Approved ProtocolsAdverse Events IdentificationProtocol DeviationsBiospecimen ResearchClinical Trials

About the role

Key responsibilities & impact

Obtain informed consent from patients using paper consent forms and REDCap e-consent platforms
Request and coordinate tissue samples through Duke Clinical Laboratories for clinical trial and research requests
Register research participants in required Duke systems
Work with leadership to ensure compliance with Duke, state, and federal regulations
Review IRB-approved protocols for regulatory and operational compliance
Assist investigators and research teams with specimen-related research activities
Participate in cross-training, including biospecimen collection and patient consenting
Assist in identifying adverse events and protocol deviations and determining reportability
Use patient health data from the Duke electronic medical record to identify cohorts, extract medical information, and access patient samples
Generate abstracts based on literature searches and reviews when participating in conferences
Ensure samples comply with CHTN quality control standards and grant milestones are met
Train new team members and contribute to training plans, group workflows, and operational design

Requirements

What you’ll need

Completion of an Associate's degree
Minimum of two years of relevant research experience
A Bachelor's degree may substitute for 2 years required experience
Highly collaborative approach and ability to set clear goals and communicate proactively and clearly with key stakeholders and staff
Commitment to completing work efficiently and by designated deadlines
Strong organizational and communication skills
Ability to use patient health data from the Duke electronic medical record
Ability to review IRB-approved protocols
Ability to comply with regulatory requirements and College of American Pathologists (CAP) guidelines

Benefits

Comp & perks

Health insurance plans
Medical and dental care programs
Generous paid time off
Retirement programs with employer contributions
Generous retirement benefits
Tuition assistance for employees and their children
Family-friendly and cultural programs
Inclusive culture valuing excellence, innovation, and discovery