Pharmacovigilance Specialist
ICON · Manila, Philippines
SafetyFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Monitor pharmaceutical product safety by collecting, analyzing, and reporting adverse events in compliance with regulatory standards. This hybrid position in Manila requires a bachelor's degree and at least 3 years of pharmacovigilance experience, including clinical trial case handling, risk assessment, and cross-functional collaboration on safety investigations.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Minimum 3 years pharmacovigilance or drug safety experience
- Hands-on experience processing and assessing pharmacovigilance cases from clinical trials
- Demonstrated ability to lead pharmacovigilance projects and manage stakeholders
- Strong analytical skills with meticulous attention to detail
- Excellent communication and collaboration abilities across teams
- Legal right to work in Philippines; hybrid work availability (2-3 days weekly in Makati)
What you'll be doing
- Collect, review, and analyze adverse event reports compliant with regulatory guidelines
- Conduct risk assessments and signal detection to identify potential safety concerns
- Collaborate with cross-functional teams on safety inquiries and investigations
- Prepare and submit safety reports and regulatory submissions on schedule
- Monitor pharmacovigilance regulations and industry best practices for safety framework enhancement
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.