Clinical Research Coordinator - Oncology
Core
Daily clinical research activities including patient recruitment, enrollment, informed consent, data collection, and protocol compliance for oncology clinical trials.
Role type
Clinical Research Coordinator (Oncology)
Builds
Clinical research protocols and data for oncology studies
Domain
Healthcare / Oncology / Clinical Research
Required skills
Patient recruitment, informed consent administration, clinical data collection and coding, regulatory compliance (IRB/FDA), adverse event monitoring, scheduling coordination, medical terminology knowledge
Preferred skills
Clinical research certification (SoCRA/ACRP), knowledge of Microsoft Office, ability to communicate with clinical staff and participants
Responsibilities
Assess patient records for eligibility, recruit and enroll patients, obtain informed consent, educate patients on study goals, coordinate patient appointments and diagnostic testing, monitor for adverse reactions, document and report unfavorable responses, collect and analyze clinical data, ensure compliance with IRB and FDA regulations, assist in developing new research protocols
Seniority
Entry-level to Mid-level, hands-on IC