Pharmacovigilance Analyst

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. The Pharmacovigilance Analyst is responsible for supporting pharmacovigilance activities to ensure compliance with global and local regulatory requirements. This role involves processing safety reports, maintaining safety databases, supporting aggregate reporting, and contributing to patient safety initiatives. Qualifications Bachelor’s degree in pharmacy or related field. 1-2 years of experience in Pharmacovigilance, Drug Safety, Regulatory Affairs, or a related field. Knowledge of local pharmacovigilance regulations, safety reporting requirements, signal management, RMP and PV system management. Experience in adverse event reporting, case management and regulatory compliance. Understanding of PV quality systems, including audits, inspections, CAPA, and SOP management. Ability to serve as the local Contact Person for Pharmacovigilance (CPPV) and liaise with Health Authorities and stakeholders. Ability to work independently, manage multiple priorities, and meet regulatory timelines. Strong communication, organizational, and stakeholder management skills. Fluent in English, both written and spoken.