PharmD-credentialed professional with European clinical experience and advanced academic research in pharmacokinetics and immunosuppressive therapies. Proficient in adverse drug reaction (ADR) evaluation, medical literature appraisal, and cross-functional scientific communication with healthcare providers. Possesses a strong foundational understanding of international regulatory frameworks, Good Pharmacovigilance Practices (GVP), and ICH-GCP guidelines. Seeking to leverage clinical judgment, drug-drug interaction (DDI) analysis, and evidence-based medicine principles to advance drug safety and medical strategy within Pharmacovigilance or Medical Affairs.