CareerPlanSign in

RN Clinical Research Oncology

Grand Rapids, MI💼 Full-time🗓 2026-07-13 → 2026-09-27

Core

Coordinate and implement clinical research studies in oncology, managing patient enrollment, data collection, and protocol compliance under Principal Investigator oversight.

Role type

Clinical Research Coordinator (Oncology)

Builds

Clinical trials for cancer research

Domain

Healthcare / Clinical Research / Oncology

Deliverable

production ML models | product features | dashboards & analysis | research

Required skills

Patient recruitment and screening, Data collection and documentation, Protocol implementation, Regulatory compliance (GCP), Budget development, IRB document preparation, Adverse event identification, Specimen handling

Preferred skills

Project management, Clinical research experience

Technologies

Electronic Data Capture (EDC) systems, Case Report Forms (CRF)

Responsibilities

Identify, recruit, screen, and enroll research subjects; Collect and document patient data into study systems; Coordinate study activities including respiratory therapy assessments and investigational product administration; Maintain compliance with federal/state laws and GCP; Prepare IRB documents and assess operational feasibility.

Seniority

Entry-level to Mid-level, hands-on IC

Sourced via workday · Listed on CareerPlan, which tracks 70,000+ jobs from 20+ sources.