Clinical Research Coord II, Oncology
Core
Mid-level coordinator supporting multiple pediatric clinical research projects with minimal supervision, managing study logistics, data collection, and regulatory compliance.
Role type
mid-level clinical research coordinator (oncology/pediatrics)
Builds
clinical trial data and specimens for pediatric oncology studies
Domain
healthcare + clinical research
Deliverable
client delivery
Required skills
study feasibility assessment, regulatory submission preparation, participant identification, data/specimen collection, record archiving, quality assurance auditing, supply management, ICH-GCP knowledge, human subjects regulatory knowledge
Preferred skills
informed consent administration, EMR system navigation, sample processing and storage
Technologies
Microsoft Office, Cerner
Responsibilities
assess feasibility of clinical research protocols, prepare materials for regulatory review and IRB submission, identify potential study participants, coordinate and collect research data and specimens, complete study records accurately, participate in quality assurance audits, manage study materials and supplies, archive records per policy
Seniority
Mid-level, hands-on IC
