

Detail-oriented Pharm D graduate with 1 year of clinical experience in an oncology department, possessing a strong foundation in pharmacovigilance, adverse event assessment, and medication safety. Skilled in reviewing and triaging patient cases, identifying potential adverse drug reactions, and ensuring accurate documentation of safety information.Experienced in collaborating with multidisciplinary teams, supporting medical monitoring activities, and maintaining high standards of data quality and compliance. Brings strong analytical skills, clinical knowledge of oncology therapies, and a commitment to patient safety, regulatory standards, and continuous learning within the pharmacovigilance field.