Pharmacovigilance Associate | Hybrid, Philippines

ICON Clinical Research; Manila; Hybrid; PHP 600,000 - 900,000; Full time

Job summary

ICON Clinical Research is hiring a Pharmacovigilance Associate in the Philippines with a hybrid work arrangement. You will monitor drug safety, review adverse event reports, and support regulatory submissions in a collaborative, compliant environment. A degree in a relevant field and PV experience are required.

You will work with a global team to ensure high standards of safety data collection, analysis, and reporting, contributing to patient safety and regulatory compliance.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field, required.
• Minimum 2 years' experience in pharmacovigilance or drug safety.
• Strong analytical skills with precise data collection and reporting.
• Excellent communication and interpersonal abilities for teamwork.
• Commitment to high quality, regulatory compliance in PV activities.
• Willingness to work in a hybrid setup: 2–3 days in Makati City.

Responsibilities

• Collecting and reviewing adverse event reports for timely regulatory reporting.
• Performing signal detection and risk assessments to identify safety issues.
• Collaborating with cross-functional teams on safety inquiries and investigations.
• Keeping up-to-date with pharmacovigilance regulations and best practices.
• Assisting in preparing safety reports and regulatory submissions.

Skills

Pharmacovigilance

Data analysis

Communication

Attention to detail

Collaboration

Compliance

Education

Bachelor's degree in a relevant scientific discipline

Job description

ICON Clinical Research is hiring a Pharmacovigilance Associate in the Philippines with a hybrid work arrangement. You will monitor drug safety, review adverse event reports, and support regulatory submissions in a collaborative, compliant environment. A degree in a relevant field and PV experience are required.

You will work with a global team to ensure high standards of safety data collection, analysis, and reporting, contributing to patient safety and regulatory compliance.