Shweta Sulakude

Experienced Clinical Research Coordinator with over 08 Months of expertise in clinical trials, electronic Trial Master File (eTMF) management, and regulatory-compliant documentation processes. Proven track record in implementing and maintaining eTMF systems, performing quality control checks, supporting audit and inspection readiness, and ensuring adherence to FDA, ICH-GCP, and industry standards. Adept at coordinating with cross-functional teams, training new associates, resolving document issues, and optimising workflows to enhance efficiency and inspection readiness across multiple clinical studies.