I am a well-organized, dedicated and hardworking professional who has developed a mature and responsible approach to any task that I undertake, or situation that I am presented with. I always strive to achieve the highest quality possible, at any task and in any situation. I am accustomed to working in a challenging and fast-paced environment, particularly when dealing with multiple projects and priorities at the same time. - I have more than 5 years of experience in Pharmacovigilance including medical writing of Safety Evaluation Reports medical assessment and literature triage. - Expertise in end-to-end signal management process (including signal validation, priortization, assessment, and risk classification) in collaboration with the global safety officer (GSO)- Experienced in medical writing, clinical study/trial review, literature review and its assessment with special focus on Benefit-Risk evaluations.- Expertise in writing Clinical Overviews (COs)/Safety Evaluation Report (SER)- Experienced in Benefit-Risk evaluations (BRE) for periodic Benefit Risk Evaluation Report (PBRERs) and performing signal detection activities.- Experienced in medical assessment activities (checking of Reference Safety Information [RSI] listedness, risk factors/confounders, and company causality).- Excellent knowledge of performing medical analysis of cases and analysis of PV data including cases from clinical sources, and healthcare professionals.- Experienced in performing literature triage inluding case/non-case reports.- Expertise in preparing safety management slides in collaboration with GSO.-Expertise in writing Health Hazard Evaluation (HHE) reports.