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Clinical Research Program Coordinator Jobs in Raleigh, NC

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Clinical Research Program Coordinator information

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How much do clinical research program coordinator jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for clinical research program coordinator in Raleigh, NC is $27.88, according to ZipRecruiter salary data. Most workers in this role earn between $22.64 and $30.14 per hour, depending on experience, location, and employer.

What does a clinical research program coordinator do?

A Clinical Research Program Coordinator organizes and manages clinical research studies within healthcare or academic settings. Their responsibilities include overseeing study protocols, recruiting and screening participants, ensuring regulatory compliance, coordinating with research teams and sponsors, and maintaining accurate documentation. They play a key role in ensuring the smooth operation of clinical trials and often act as a liaison between investigators, participants, and regulatory bodies.

What are the key skills and qualifications needed to thrive as a clinical research program coordinator?

To thrive as a Clinical Research Program Coordinator, you need a background in life sciences or healthcare, experience with research protocols, and often a bachelor’s or master’s degree in a related field. Familiarity with regulatory compliance, data management systems like REDCap, and certifications such as CCRC or ACRP are typically required. Strong organizational skills, attention to detail, and effective communication help coordinate teams and ensure protocol adherence. These skills are vital for maintaining research integrity, meeting regulatory standards, and ensuring successful project outcomes.

What are the main challenges clinical research program coordinators face when managing multiple studies simultaneously?

Clinical Research Program Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring regulatory compliance, and maintaining clear communication across diverse teams. Effective time management and organizational skills are critical, as coordinators must track study progress, manage documentation, and resolve any issues that arise promptly. Collaborating closely with principal investigators, research staff, and external partners is essential to keep studies running smoothly and maintain high standards of data integrity.

What is the difference between Clinical Research Program Coordinator vs Clinical Research Associate?

AspectClinical Research Program CoordinatorClinical Research Associate
CredentialsOften requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonTypically requires a bachelor's degree; certifications like CRA or RAC are beneficial
Work EnvironmentManages study logistics, coordinates between teams, and oversees daily operations at research sitesMonitors clinical trials at multiple sites, ensuring compliance and data integrity
Employer & Industry UsageUsed by hospitals, research institutions, and pharmaceutical companies for site managementEmployed mainly by CROs and pharmaceutical companies for trial monitoring

While both roles support clinical research, the Clinical Research Program Coordinator focuses on site management and daily operations, whereas the Clinical Research Associate primarily monitors trial progress across sites to ensure compliance and data quality.

What are the most commonly searched types of Clinical Research Program jobs in Raleigh, NC?

The most popular types of Clinical Research Program jobs in Raleigh, NC are:

What are popular job titles related to Clinical Research Program Coordinator jobs in Raleigh, NC?

For Clinical Research Program Coordinator jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Research Program Coordinator jobs in Raleigh, NC look for?

The top searched job categories for Clinical Research Program Coordinator jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Research Program Coordinator jobs?

Cities near Raleigh, NC with the most Clinical Research Program Coordinator job openings:

Infographic showing various Clinical Research Program Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $58,000 per year, or $27.9 per hour.

Clinical Research Nurses Coordinator - Duke Cancer Institute

Duke Clinical Research Institute

Durham, NC • On-site

$62K - $78K/yr

Other

Medical, Dental, Retirement

Posted 13 days ago


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.

Duke Cancer Institute (DCI) is seeking an Oncology Clinical Research Nurse Coordinator (CRNC) to join the Cancer Control & Population Science (CCPS) Clinical Research Program. In this unique role, you will support innovative oncology clinical trials focused on supportive care, survivorship, and navigation interventions that improve the lives of patients and families across the cancer continuum.

As a Clinical Research Nurse Coordinator, you will serve as the nurse navigator for clinical trials involving oncology nurse navigation interventions. You will work with diverse oncology populations participating in NIH-funded, industry-sponsored, and investigator-initiated research studies with complex multidisciplinary protocols. As part of Duke Cancer Institute's shared research infrastructure, you will collaborate closely with investigators, study teams, and clinical partners to ensure the consistent delivery of patient navigation services and successful implementation of clinical research studies.

This position combines the rewarding aspects of oncology nursing, patient navigation, and clinical research. You will work directly with patients and families to identify barriers to care, provide education and support, facilitate informed decision-making, and coordinate services across multidisciplinary teams following the study-specific protocols while contributing to research that advances supportive care and survivorship outcomes.

Minimum Requirements

  • Graduation from an accredited BSN program, Associate Degree in Nursing program, or Nursing Diploma program
  • Current Registered Nurse (RN) licensure in North Carolina or compact state licensure
  • Basic Life Support (BLS) certification required
  • Minimum of twelve months of clinical nursing experience
  • Ability to utilize Microsoft Office products, web-based applications, and electronic clinical research systems
  • Ability to maintain compliance with required hospital, unit, research, and nursing competency requirements

Preferred Qualifications

  • Oncology nursing experience
  • Clinical research experience
  • Nurse navigation experience
  • Experience working within multidisciplinary oncology care teams
  • Knowledge of clinical trial operations, informed consent procedures, and regulatory requirements
  • Experience supporting NIH-funded, investigator-initiated, or industry-sponsored clinical studies
  • Familiarity with Electronic Data Capture (EDC) systems and clinical research documentation

Other Requirements

  • Maintain active RN licensure and compliance with North Carolina Board of Nursing requirements
  • Maintain all Duke-required clinical research, institutional, and nursing certifications and training
  • Ability to work effectively with diverse patient populations experiencing complex medical, psychosocial, and health-related social needs
  • Ability to communicate professionally and effectively with patients, caregivers, investigators, sponsors, and multidisciplinary clinical teams

Be Bold.

Coordinate Complex Oncology Clinical Trials

  • Coordinate multiple oncology clinical trials and research studies supporting the Duke Cancer Institute's Supportive Care and Survivorship Center and related oncology research programs.
  • Recruit, screen, consent, enroll, schedule, and manage study participants throughout the research lifecycle.
  • Coordinate study visits, maintain regulatory documentation, manage enrollment records, report adverse events, and ensure compliance with protocol requirements, institutional policies, and applicable regulations.
  • Evaluate study recruitment and retention performance and develop strategies to improve participant engagement and study success.

Provide Oncology Nurse Navigation and Care Coordination

  • Deliver comprehensive oncology nurse navigation services for patients enrolled in clinical trials involving nurse-led navigation interventions.
  • Assess clinical, psychosocial, educational, and supportive care needs of oncology patients and caregivers.
  • Identify barriers to care, facilitate access to treatment and supportive services, and collaborate with multidisciplinary teams to improve care coordination and continuity.
  • Provide education, advocacy, symptom management support, treatment adherence guidance, and assistance with informed decision-making throughout the cancer continuum.

Manage Study Data and Research Compliance

  • Utilize Electronic Data Capture (EDC) systems to ensure accurate and timely study data entry.
  • Identify and resolve data quality issues, missing documentation, and compliance concerns.
  • Maintain data integrity, confidentiality, security, and regulatory readiness across assigned studies.
  • Assist with audits, monitoring visits, and study quality assurance activities.

Serve as a Collaborative Research and Clinical Resource

  • Act as the primary liaison between investigators, sponsors, study teams, and participants for assigned clinical trials.
  • Participate actively in program meetings, committees, working groups, and research initiatives.
  • Serve as a resource for colleagues regarding oncology nurse navigation, clinical trial operations, patient-centered care, and research best practices.
  • Support consistent implementation of nurse navigation interventions across multiple research protocols.

Promote Ethical Conduct of Research

  • Educate patients and research staff regarding the distinction between clinical care and research participation.
  • Ensure informed consent processes are conducted ethically and in accordance with regulatory requirements.
  • Maintain compliance with Good Clinical Practice (GCP), institutional policies, study protocols, and research regulations.
  • Support a culture of ethical research conduct, patient safety, and participant advocacy.

Choose Duke.

At the Duke Cancer Institute, discovery and compassion come together to transform cancer care. As one of the nation's leading cancer centers, DCI brings together world-class researchers, clinicians, and healthcare professionals dedicated to advancing cancer prevention, treatment, survivorship, and supportive care through innovative research and patient-centered care.

This position offers a unique opportunity to work at the intersection of oncology nursing, patient navigation, and clinical research. You will help shape the future of supportive cancer care by contributing to nurse-led navigation interventions and multidisciplinary research initiatives designed to improve patient outcomes and reduce barriers to care.

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 $66,265.00 to USD $107,096.00. 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, sex (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).