Swati Bhattacharya

WORK HISTORY

EDUCATION

ABOUT SWATI BHATTACHARYA

I am Swati Bhattacharya, a dedicated Senior Clinical Research Associate with 3+ years of experience in the clinical research domain, actively involved in managing clinical trials, ensuring protocol compliance, and maintaining high-quality data standards. I have a strong academic background in Life Sciences and a growing passion for clinical development and patient safety.With hands-on experience in site monitoring, documentation, and regulatory communication, site management. I bring a focused and systematic approach to each study I support. My goal is to contribute to the development of safe, effective, and innovative medical therapies.Key Skills and Knowledge:• Clinical Guidelines and Protocols.• eTMF and Clinical Trials (Phases and Types).• Clinical Trial Management & Site Coordination.• ICH-GCP Guidelines and NDCT Rules (2019).• Clinical Study Report (CSR).• Electronic Data Capture (EDC).• Adverse Drug Reactions and Events (including Serious Adverse Event).• Reporting Timelines and Ethics Committee Procedures.• Regularly Authority Interaction.• Pharmacokinetics Parameters and Bioequivalence Analysis.• Basic understanding of SOP and Guidelines Terminology.Additionally, I possess basic proficiency in MS Excel, which aids in Data Management and Analysis.I am driven by the mission of improving healthcare outcomes through responsible and efficient clinical research practices. Always open to new opportunities, collaborations, and professional connections within the pharmaceutical and clinical research industry.