A Clinical Research Professional who contributes to the planning, execution, and monitoring of clinical trials in various therapeutic areas. I am capable of applying my skills in carrying out pharmacovigilance activities and corrective and preventive action (CAPA) to ensure the quality and safety of the trials. I also support data management, documentation, and communication processes with internal and external stakeholders. Prior to that, I worked as a Pharmacist/Safety Specialist where I provided drug information and dispensed medications to Patients while ensuring safety through compliance and administration, also reviewed adverse event reports. With over four years of combined experience in the clinical research and pharmacy fields, I am a competent and reliable professional who strives to improve the health outcomes and well-being of people through ethical and evidence-based practices.