Sradha

Clinical Data Coordinator / Assistant

Supported clinical data collection and entry across study records, maintaining accuracy and completeness of study-related information in line with protocol requirements.. Performed data quality validation and review to identify discrepancies, raise queries, and support reliable, audit-ready clinical data.. Assisted with regulatory compliance and clinical research documentation in accordance with applicable procedures, sponsor requirements, and GCP guidelines.. Followed established Standard Operating Procedures (SOPs) for clinical research activities and documentation control.. Assisted in tracking and monitoring adverse events and safety-related data, supporting timely and accurate safety reporting.