8+ years of experience in Pharmacovigilance including both drug and device case processing. 5 years of experience as Safety lead for clinical trials from different therapeutic areas ((Intervention Cardiology, Cardiac Rhythm Management, Peripheral Intervention and Oncology). Experienced in processing Safety data according to applicable regulations, guidelines, procedures and project requirements. Experience in Start-up activity, Conduction phase and Close out activity. Experience in collaborating with other stakeholders and setting-up of Safety databases as per the study requirement and performing User Acceptance Testing for the same. Experience in client interactions, understanding client expectations and meeting the deliverables on time. Capable and committed lead with a proven ability to meet agreed deadlines, workload management and team management.