Remote Pharmacovigilance Safety Surveillance Specialist

ProPharma; Makati; Hybrid; PHP 600,000 - 900,000; Full time

Job summary

ProPharma, based in the Philippines, seeks a Pharmacovigilance Safety Surveillance Specialist to ensure effective case processing for adverse events from clinical trials and post-marketed products. The role emphasizes MedDRA coding, seriousness assessment, and timely, regulatory-compliant deliverables.

Ideal candidates have 2+ years in pharmacovigilance, with end-to-end PV experience and literature screening.

Qualifications

• 2+ years of experience in pharmacovigilance.
• Knowledge of end-to-end PV case processing (clinical and post-market).
• Experience with literature screening activities.

Responsibilities

• Oversee and perform daily adverse event case processing, including coding with MedDRA and assessing seriousness and expectedness.
• Perform follow-up activities to collect necessary information.
• Create and review case narratives and provide client notifications as required.
• Conduct literature searches and monitor Health Authority websites.
• Ensure deliverables comply with regulatory requirements and are sent within timelines.
• Support updating project-related documents and regulatory intelligence activities.

Skills

Strong communication

Attention to detail

Problem solving

Teamwork

Organizational skills

PV knowledge

Education

Bachelor’s degree in life sciences or health-related field

Advanced degree / RN / RPh / PharmD (preferred)

Tools

Oracle Argus Safety

ARISg

Other PV databases

Job description

ProPharma, based in the Philippines, seeks a Pharmacovigilance Safety Surveillance Specialist to ensure effective case processing for adverse events from clinical trials and post-marketed products. The role emphasizes MedDRA coding, seriousness assessment, and timely, regulatory-compliant deliverables.

Ideal candidates have 2+ years in pharmacovigilance, with end-to-end PV experience and literature screening.