Dynamic Study Coordinator with over two years of experience in oncology clinical trials (Phases 1-3), skilled in managing study protocols and ensuring compliance with regulatory standards. Expertise in data collection, analysis, and reporting, with a strong emphasis on maintaining quality and efficiency. Proven ability to collaborate effectively with CROs, seeking to transition into a Clinical Research Associate role to broaden responsibilities and enhance contributions to clinical trial management from the sponsor/CRO perspective. Committed to advancing the field of clinical research through meticulous attention to detail and a proactive approach to problem-solving.
Phase 1, 2, 3 oncology trials
Clinical trial coordination ( participant recruitment , screening, and scheduled visits)
GCP compliance
Patient safety and Protocol adherence
Adverse event tracking and reporting
CRF and EDC systems: Experienced with Medidata Rave, InForm, and Veeva Vault; familiar with Oracle EDC and TrialMax
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