Job detail

Clinical Research Nurse-Lymphoma

City of Hope

#Case Management #FDA #BLS Certification #RN License #Clinical Research #BSN #Oncology #Patient-Centered Care #IRB #Nurse Navigation

Quick overview

Manage clinical trial patients by assessing eligibility, monitoring treatment responses, and ensuring strict adherence to IRB protocols. Coordinate care across multidisciplinary teams and educate patients and families on trial procedures and informed consent.

Requirements summary

Requires a BSN and a current California RN license with BLS certification. Candidates must have at least 2 years of experience in oncology, clinical research, ICU, or related intensive care settings.

bachelor degreeCase ManagementPatient MonitoringPatient AssessmentRegulatory CompliancePatient EducationClinical DocumentationTriageOncology NursingInformed ConsentClinical Trial ManagementRandomizationIRB Protocol Compliance

Job description

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix.
Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.
Are you a compassionate and detail-oriented Registered Nurse passionate about advancing healthcare?
Join our team as a Clinical Research Nurse, where you’ll play a vital role in guiding patients through innovative clinical trials while collaborating with a multidisciplinary team of physicians, Clinical Research Associates (CRA), pharmacists, and coordinators.
This is a unique opportunity to blend clinical expertise with research excellence—helping bring groundbreaking treatments to life while delivering exceptional patient-centered care.
What You’ll Do Clinical Trial Patient Management Partner with investigators to determine patient eligibility and ensure accurate documentation of clinical trial criteria Assess, monitor, and document patient conditions, treatment responses, and changes in health status in accordance with IRB protocols Coordinate care across the continuum (outpatient, inpatient, and home settings) Triage patient calls and provide proactive communication and support to patients and families Collaborate closely with physicians, nurse practitioners (NPs), physician assistants (PAs), pharmacists, and research teams Plan and execute protocol-specific activities including randomization, assessments, treatments, and follow-ups Ensure all clinical trial documentation is complete, accurate, and compliant to avoid protocol deviations Support and monitor patient adherence to study protocols Patient & Family Education Educate patients and families on clinical trial treatments, procedures, and follow-up care Provide ongoing support to ensure understanding and adherence to treatment plans Informed Consent & Compliance Ensure informed consent processes meet all regulatory requirements (IRB, FDA, institutional, and sponsor guidelines) Participate in patient education during consent and escalate concerns to the Principal Investigator Maintain timely and accurate documentation of consent forms Protocol Oversight & Collaboration Assist with study initiation, monitoring visits, and audits Collaborate with research pharmacy and investigators to develop and implement protocol-specific orders Promote adherence to clinical trial protocols and regulatory standards Coordinate scheduling of patient visits, testing, and follow-ups Educate nursing staff on protocol requirements and safe medication administration Additional Responsibilities Deliver patient-centered care in alignment with organizational policies and the California Nurse Practice Act Maintain a high standard of professionalism, teamwork, and organization Stay current with clinical research regulations, standards, and best practices Serve as a mentor or preceptor for new staff and nursing students Collaborate with internal teams and external partners including physicians, sponsors, and community resources Part time 3-10 hour shifts / 30 hours per week

Clinical Research Nurse-Lymphoma

Quick overview

Requirements summary

Job description

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