Kaiser PermanenteClinical Research Coordinator
Jan. 2025United StatesEnsured compliance with Kaiser Permanente’s Code of Conduct, IRB SOPs, and regulations (GCP, federal, state, local) while supporting inspections, audits, and monitoring visits.
Managed participant data security, coordinated study visits, and collected/report data according to protocol, ensuring timely communication with the Principal Investigator (PI).
Assisted with participant recruitment, medical record reviews, and data abstraction, maintaining accurate case report forms and tracking study activities.
Coordinated specimen shipping, long-term follow-up data collection, and study closure activities.
Communicated with internal and external stakeholders to ensure regulatory compliance and maintained essential trial documents.