Ankita Vaidya

WORK HISTORY

EDUCATION

SKILLS

ABOUT ANKITA VAIDYA

Drug safety professional with nearly 10.5 years of qualitative experience in Clinical Safety and Pharmacovigilance. Skilled in ensuring compliance with applicable regulations or SOPs; specializes in drug safety management, clinical trials and medical supervision. Expertise in conducting, monitoring & reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and adverse effects or side effects of drug products. Excellent in monitoring all products and conducting post-market evaluations to ensure drug safety; assessing adverse event, updating safety narratives, conducting quality and conveying drug related case reports to appropriate authorities. Adept in conducting and supervising regular pharmacovigilance processes; attending several product safety meetings and adding functionality to product safety. Constantly engaged in global pharmacovigilance activities to support data safety and case tracking; perform document archiving; assist in the administration of pharmacovigilance meetings; support quality of review documents and initiate business liaison. Capable of monitoring safety literature to stay current on the latest safety information related to the company\'s products. Strong exposure in providing oversight of SAE reconciliation activities between the clinical and safety databases in accordance with SOPs. Strong people and project leadership skills with excellent analytical and problem solving abilities. If you wish to know more about my experience or can think of me being an asset to your organization, then please DM or contact me at a••••••••@gmail.com.