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Clinical Research Coder Jobs in Raleigh, NC (NOW HIRING)

Research Assistant

Raleigh, NC · On-site

$18.12 - $25.51/hr

Summary: Screens and enrolls patients in clinical trials, conducts all patient follow-up ... DATA CODING-GENERAL; DATA ANALYSIS/INTERPRETATION. REASONING ABILITY Ability to apply common sense ...

The Clinical Data Manager will apply his or her knowledge of Clinical Research, therapeutic areas ... Develops project-specific eCCG, data management plans that address areas such as data coding ...

Reviews the complex (problematic coding that needs research and reference checking) medical records ... Correlate information from "approved" supporting clinical documentation, not limited to pathology ...

Reviews the complex (problematic coding that needs research and reference checking) medical records ... Correlate information from "approved" supporting clinical documentation, not limited to pathology ...

Reviews the complex (problematic coding that needs research and reference checking) medical records ... Correlate information from "approved" supporting clinical documentation, not limited to pathology ...

Reviews the complex (problematic coding that needs research and reference checking) medical records ... Correlate information from "approved" supporting clinical documentation, not limited to pathology ...

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Clinical Research Coder information

See Raleigh, NC salary details

$18

$29

$41

How much do clinical research coder jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for clinical research coder in Raleigh, NC is $29.31, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $31.06 per hour, depending on experience, location, and employer.

What does a Clinical Research Coder do?

A Clinical Research Coder is responsible for reviewing clinical research documentation and assigning standardized medical codes to diagnoses, procedures, and treatments. This role ensures that data collected during clinical trials is accurately coded for analysis, reporting, and regulatory compliance. Clinical Research Coders work closely with clinical research teams to maintain data integrity, support billing processes, and facilitate research outcomes. They must be familiar with medical terminology, coding systems such as ICD and CPT, and regulatory requirements related to clinical trials.

How does a Clinical Research Coder typically interact with clinical research teams and principal investigators?

Clinical Research Coders work closely with clinical research teams, including principal investigators, study coordinators, and data managers, to ensure that medical procedures and diagnoses are accurately translated into standardized codes. These professionals often participate in regular meetings to clarify clinical documentation, resolve coding discrepancies, and ensure adherence to regulatory and billing requirements. Their collaborative efforts help maintain data integrity and compliance, supporting the smooth operation of research studies and the accurate reporting of outcomes.

What are the key skills and qualifications needed to thrive as a Clinical Research Coder, and why are they important?

To thrive as a Clinical Research Coder, you need a strong understanding of medical terminology, coding systems (like ICD-10 and CPT), and clinical research protocols, often supported by a degree in health information management or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as Certified Professional Coder (CPC) are commonly required. Attention to detail, analytical thinking, and effective communication skills help ensure accurate data coding and collaboration with research teams. These skills and qualifications are essential for maintaining data integrity, regulatory compliance, and efficient clinical research operations.

What is the difference between Clinical Research Coder vs Clinical Data Coordinator?

AspectClinical Research CoderClinical Data Coordinator
CredentialsCertification in medical coding, clinical research experienceOften requires clinical data management training, sometimes certifications
Work EnvironmentResearch sites, hospitals, clinical trial settingsData management departments, research organizations
Employer & IndustryPharmaceutical companies, research institutionsHospitals, research organizations, CROs
Primary FocusAccurate coding of clinical trial dataManaging and ensuring data quality and integrity

While both roles support clinical research, Clinical Research Coders focus on coding and classifying clinical trial data, whereas Clinical Data Coordinators manage overall data collection and quality assurance. Both positions require knowledge of clinical terminology and data management, but their daily tasks and responsibilities differ.

What cities near Raleigh, NC are hiring for Clinical Research Coder jobs? Cities near Raleigh, NC with the most Clinical Research Coder job openings:
Clinical Research Nurse Coordinator - Duke Cancer Institute

Clinical Research Nurse Coordinator - Duke Cancer Institute

Duke University

Durham, NC • On-site

$66K - $83K/yr

Full-time

Medical, Dental, Retirement

Posted 17 days ago


Duke University rating

6.5

Company rating: 6.5 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

436th of 535 rated colleges and universities


Job description

School of Medicine:
Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.
Be You.
You will provide leadership and coordination for multiple, complex oncology clinical trials-including investigational products (IP)-within the Duke Cancer Institute's Bone Marrow Transplant, Hematology Malignancies & Cellular Therapy Clinical Research Program [BMT]. You'll collaborate with the Oncology Clinical Research Unit (CRU), Principal Investigators (PIs), sponsors, and study teams to ensure feasibility, compliance, and participant-centered care. Daily, you will recruit and consent participants, conduct study visits, maintain regulatory documentation, and troubleshoot challenges to keep studies on track.
Your work spans operations, site management, communication, data integrity, leadership, and ethics. If you thrive in complex neuro-oncology research, enjoy mentoring others, and want to advance breakthrough therapies for brain tumor patients, this role is for you.
Minimum Requirements:
  • Education: Graduation from an accredited BSN or Associate Degree in Nursing or Nursing Diploma program. Registered nurses without a BSN must enroll within two years and complete within seven years of start date.
  • Licensure/Certifications: Current or compact RN licensure in North Carolina; BLS required; maintain active NCBON status and hospital/unit competencies.
  • Experience: Minimum of 12 months of appropriate clinical nursing experience.

Preferred Qualifications:
  • Oncology and/or clinical research experience.
  • Familiarity with EDC systems, investigational product handling, and Good Clinical Practice (GCP).
  • Experience coordinating multi-stakeholder studies and supporting site initiation/closeout.

Other Requirements:
  • On-call: Overnight and/or weekend call for Convection-Enhanced Delivery (CED) infusions.
  • Clinical competencies: Ambulatory medication administration, medication education and management, adult chemotherapy administration, basic dysrhythmia review, lab result review, adverse event assessment, and patient education.
  • Ability to interact effectively with multidisciplinary teams and support patient compliance.
  • Compliance: Maintain Duke and project-specific training and certification requirements; follow SOPs, regulations, and protocol requirements governing clinical research.

Be Bold.
  • Direct study operations for multiple complex neuro-oncology trials, including feasibility assessments, recruitment and retention strategies, informed consent, scheduling, and execution of participant visits.
  • Coordinate site management activities (initiation through closeout), maintain regulatory binders and study-level documentation, manage delegation of authority logs, record and report adverse events (AEs), and ensure compliance with institutional policies and SOPs.
  • Serve as the primary liaison among sponsors, PIs, CRU, monitors, and study personnel; communicate clearly and escalate issues appropriately to drive timely resolution.
  • Ensure high-quality data capture in EDC systems; recognize and troubleshoot data issues; uphold data security and provenance standards and support query resolution.
  • Partner with finance teams on study payments, participant care expense workflows, and budget development; monitor financial milestones and assist with study budget closeouts.
  • Provide RN-level clinical support aligned with protocol (e.g., ambulatory medication administration, adult chemotherapy administration, adverse event assessment, laboratory review, patient education, and CED infusion call coverage).
  • Lead and mentor colleagues; actively participate in team meetings, committees, task forces, and ad hoc groups; contribute to scientific presentations and publications.
  • Model research ethics: clearly communicate the distinction between clinical care and research activities to staff and participants; summarize and clarify applicable professional guidelines and codes of ethics.

Choose Duke.
Join a mission-driven team within the Duke Cancer Institute's Bone Marrow Transplant, Hematology Malignancies & Cellular Therapy Clinical Research Program, where discovery, collaboration, and patient-centered care drive everything we do. You will work alongside leading investigators, research nurses, coordinators, and data experts focused on advancing therapies for patients with brain tumors.
You'll find robust professional development and mentorship opportunities, the chance to contribute to scientific presentations and publications, and a culture committed to inclusion and excellence
Job Code: 00001203 CLINICAL RESEARCH NURSE COORDINATOR
Job Level: 54
Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $64,966.00 to USD $104,996.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.
Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/
Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, (including pregnancy and pregnancy related conditions), sexual orientation, or military status.
Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.
Essential Physical Job Functions:
Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

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About Duke University

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Duke is regarded as one of America's leading research universities. Located in Durham, North Carolina, Duke is positioned in the heart of the Research Triangle, which is ranked annually as one of the best places in the country to work and live. Duke has more than 15,000 students who study and conduct research in its 10 undergraduate, graduate, and professional schools. With about 40,000 employees, Duke is the third largest private employer in North Carolina, and it now has international programs in more than 150 countries.

Industry

Colleges, universities, and professional schools and hospitals

Company size

10,000+ Employees

Headquarters location

Durham, NC, US