Data Coordinator - Full Time - Wolf River
Core
Manage clinical trial data for study subjects by completing case report forms, resolving data queries, and supporting monitoring visits.
Role type
Clinical trial data coordinator
Builds
Clinical trial data packages for sponsors and regulatory bodies
Domain
Healthcare / Clinical Research
Required skills
Case report form (CRF) management, data query resolution, regulatory compliance (GCP/ICH/FDA), medical documentation interpretation, project timeline development, audit preparation, stakeholder liaison, Microsoft Excel/Word proficiency
Preferred skills
Medical terminology, health information management experience
Responsibilities
Complete CRFs using source documents or EMR, generate and follow up on data queries, schedule and oversee sponsor monitoring visits, review CRF entries for accuracy, maintain subject screening/enrollment logs, prepare for study audits, attend investigator and sponsor meetings
Seniority
Mid-level, hands-on IC