Healthcare professional offering over 2 years of comprehensive pharmacovigilance and drug safety monitoring experience in pharmaceutical and clinical trials. Well-versed with medical terminology and medical conditions to evaluate the effectiveness, side effects, and safety of drugs. Skilled in interviewing and recruiting clients for clinical trial studies in compliance with ICH and GCP guidelines. Proven expertise in case management of adverse event records from triage, coding to analysis phases while collecting adverse events in centralized databases and reviewing public research literature. Demonstrated excellent communication and presentation skills to provide training to new employees, vendors, and business partners, which promoted job satisfaction, increased product awareness, and improved sales. Utilized analytical and critical thinking skills for conducting pre-clinical, clinical, and post-marketing drug safety reviews in accordance with local and international regulations, guidelines, and applicable directives. Proficient in Microsoft Office, and Drug Safety Databases.Strong educational background with Bachelor’s degree in Dental Surgery and a Master’s degree in Clinical Research.