I hold a Master's in Public Health from the University of Bedfordshire, United Kingdom, and a Doctorate in Pharmacy (PharmD) from Rajiv Gandhi University of Health Sciences, India. My academic foundation has equipped me with a strong understanding of healthcare systems, public health principles, and pharmaceutical sciences, which I have applied throughout my professional career.I have over four years of experience in the pharmaceutical industry, with a focus on pharmacovigilance and medical writing. Most recently, I worked as a Scientific Writer at Tata Consultancy Services, where I developed regulatory documents such as Clinical Study Reports (CSRs), Periodic Safety Update Reports (PSURs), and Risk Management Plans (RMPs) for global pharmaceutical clients. Prior to this, I worked as a Drug Safety Associate at Accenture, where I handled the end-to-end process of pharmacovigilance, ensuring regulatory compliance and supporting patient safety initiatives.Looking ahead, my goal is to continue advancing in the field of pharmacovigilance, with the aim of becoming a Director of Pharmacovigilance. I am eager to lead cross-functional teams, manage key client relationships, and drive the safety and regulatory processes that ensure patient well-being, while contributing to the strategic growth of an organization. I am committed to delivering excellence in drug safety and regulatory affairs, and I look forward to the opportunity to make a significant impact in the pharmaceutical industry.