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Duke University

Private research university in Durham, NC

Clinical Research Nurse Coordinator - Duke Cancer Institute

Full-Time
$66.3k - $107.1k/yr
Junior
Bachelor's, Associate's
Durham, NC, USA
In Person
Medical, Clinical & VeterinaryNursing & Frontline Patient Care

About the job

Requirements
  • Graduation from an accredited Bachelor of Science in Nursing program, Associate Degree in Nursing program, or Nursing Diploma program.
  • Current Registered Nurse licensure in North Carolina or compact state licensure.
  • Basic Life Support certification is required.
  • At least twelve months of clinical nursing experience.
  • Ability to use Microsoft Office products, web-based applications, and electronic clinical research systems.
  • Ability to maintain compliance with required hospital, unit, research, and nursing competency requirements.
  • Active Registered Nurse licensure and compliance with North Carolina Board of Nursing requirements.
  • Ability to 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.
Responsibilities
  • 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.
  • 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.
  • Use Electronic Data Capture 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.
  • 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.
  • 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, institutional policies, study protocols, and research regulations.
  • Support a culture of ethical research conduct, patient safety, and participant advocacy.
Desired 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 systems and clinical research documentation.

About the company

Duke University is a research university offering undergraduate, graduate, and professional education alongside interdisciplinary research and health care.

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