Clinical Research Coordinator I, Oncology
Core
Manage pediatric clinical research studies by coordinating protocols, recruiting participants, collecting data/specimens, and maintaining regulatory compliance.
Role type
Clinical Research Coordinator I (Oncology)
Builds
Clinical trials for pediatric oncology patients
Domain
Healthcare / Clinical Research / Oncology
Deliverable
client delivery
Required skills
Clinical research coordination, IRB submission preparation, participant recruitment, data collection, quality assurance auditing, source document development, ICH-GCP knowledge, Microsoft Office proficiency
Preferred skills
Informed consent administration, Cerner EMR knowledge, sample processing and storage, pediatric research experience, hospital setting experience
Responsibilities
Assess feasibility of clinical research protocols, prepare materials for regulatory review and IRB submission, identify potential study participants, collect research data and specimens, complete study records, participate in quality assurance audits, manage study materials and supplies, coordinate research team meetings
Seniority
Entry-level IC
