As a pharmacovigilance professional with over 6 years of experience, I have a strong background in clinical research, drug development, and safety regulations. Holding a master's degree in pharmacy (Pharmaceutics), I have worked extensively in the industry and have taken on a variety of roles, including Senior Safety Data Analyst, Subject Matter Expert, and mentor for global PV process.In addition to my experience, I have knowledge of QMS systems, and I have demonstrated my leadership skills by guiding my team in identifying and implementing solutions to quality and compliance issues. My effective communication skills and attention to accuracy and detail helps me process ICSRs with great efficiency.I am passionate about continuing to learn new strategies and methodologies to improve my work and stay up to date with the latest developments in the field. Overall, I am committed to providing high-quality work and taking a leadership role in challenging assignments.