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. 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.