About this role
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.