Clinical Research Nurse I
Core
Coordinate oncology clinical trials, manage patient recruitment and consent, conduct study procedures, and ensure site compliance with GCP guidelines.
Role type
Clinical Research Nurse I (Oncology)
Builds
Clinical trials for oncology patients
Domain
Healthcare / Oncology / Clinical Research
Required skills
RN license, BLS certification, clinical trial coordination, patient recruitment, informed consent, data documentation, adverse event reporting, specimen collection, regulatory compliance, patient education, 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 select study participants; obtain and document informed consent; conduct study-related procedures and assessments; document medical data and adverse events; coordinate specimen collection; provide patient education; update CTMS; liaise with investigators, sponsors, and auditors.
Seniority
Mid-level, hands-on IC
