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. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Pharmacovigilance Analyst.

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