PA
ParexelPharmacovigilance Analyst
LocationThailand-Bangkok
Typefull-time
SeniorityEntry
Experience1–2 yrs
Company size10,000+ people
PostedSep 23, 2026 · 2w ago
Verified live18h ago
At a glanceSummarised by Seekless from the posting.
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
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.