Clinical Research Nurse II
Core
Coordinate clinical research studies for oncology, hematology, radiation oncology, and blood and marrow transplant patients, ensuring protocol compliance and patient safety.
Role type
Clinical Research Nurse II (IC)
Builds
Clinical trial execution and patient recruitment for early-phase and multi-centered oncology trials
Domain
Healthcare / Oncology / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial coordination, patient screening and eligibility assessment, informed consent process management, protocol compliance monitoring, data collection and case report form completion, adverse event reporting, staff training on study protocols, patient recruitment strategy implementation
Preferred skills
ACRP or SoCRA certification, Oncology Certified Nurse (OCN) designation
Technologies
Electronic health records, Clinical trial management systems, IRB submission platforms
Responsibilities
Coordinate logistics of patient visits and clinical activity including test scheduling; Screen potential patients and assess eligibility based on clinical history and functional status; Ensure compliance with research protocols and Good Clinical Practice guidelines; Submit accurate protocol data, case report forms, and serious adverse events to IRB, sponsors, and FDA; Educate patients and families regarding clinical trial details; Organize protocol inservices for staff to ensure understanding of study specifics
Seniority
Mid-level, hands-on IC