Clinical Research Nurse 1
Core
Coordinate oncology clinical trials, manage patient recruitment and consent, conduct study procedures, and ensure site compliance with protocols.
Role type
Clinical Research Nurse (IC)
Builds
Clinical trial data and patient care continuity for oncology studies
Domain
Healthcare / Oncology Clinical Research
Required skills
RN license, BLS certification, clinical trial coordination, patient recruitment, informed consent, data documentation, protocol compliance, specimen collection, adverse event reporting, staff training
Preferred skills
Oncology experience, inpatient/ICU experience, clinical research experience, GCP knowledge
Technologies
CTMS
Responsibilities
Coordinate assigned clinical trials throughout the lifecycle; recruit and screen study participants; obtain informed consent; conduct study procedures and assessments; manage patient communication and symptom triage; document medical data and adverse events; coordinate specimen collection; provide patient education; conduct staff training; liaise with investigators, sponsors, and auditors.
Seniority
Mid-level, hands-on IC
