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.