Pharmacovigilance Safety Surveillance Specialist

Location: Makati City, Philippines

Company

hirify.global provides consulting and operational solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology for biotech, medical device, and pharmaceutical organizations.

What you will do

• Process and oversee daily clinical trial and post-market adverse event cases.
• Code cases using MedDRA and assess seriousness and expectedness at event and case level.
• Perform follow-up activities, identify missing information, and create and review case narratives.
• Conduct literature searches and monitor Health Authority websites.
• Provide client notifications and deliver compliant case-processing outputs within agreed timelines.
• Reconcile process trackers, maintain project documents, and support Regulatory Intelligence activities.

Requirements

• Bachelor’s degree in life sciences, a health-related field, or equivalent qualification and experience.
• At least 2 years of pharmacovigilance experience, including clinical and post-market end-to-end case processing.
• Experience with literature screening activities.
• Intermediate knowledge of pharmacovigilance and working knowledge of safety systems such as Oracle Argus Safety, ARISg, or similar databases.
• Strong communication, organizational, problem-solving, accuracy, and attention-to-detail skills.
• Ability to work professionally within a multidisciplinary team.

Nice to have

• Advanced degree, RN, RPh, PharmD, or equivalent qualification.

Culture & Benefits

• Commitment to diversity, equity, inclusion, and an equal-opportunity workplace.
• Encouragement of innovative, collaborative, and entrepreneurial contributions.
• Remote working is supported across the company, while employees near an office may be encouraged to work on a hybrid basis by agreement with their manager.
• Applications are reviewed personally by the recruitment team rather than AI screening tools.