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Pharmacovigilance Specialist
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Getz Pharma Philippines seeks an experienced Pharmacovigilance Specialist to ensure the safety and quality of our products. The successful candidate will be responsible for overseeing the collection, assessment, and reporting of adverse events in compliance with local and international regulatory requirements.
The ideal candidate will have a strong background in pharmacovigilance, with experience in managing risk assessments, submitting safety reports, and collaborating with cross-functional teams.
Key Responsibilities- Responsible for immediately reporting all adverse events related to our products, as per local regulation.
- Conduct risk assessments and prepare assessment reports using tools such as the Naranjo Scale.
- Maintain a comprehensive database of all reported adverse events and continuously monitor for any trends or patterns.
- A minimum of 3-5 years of experience in Pharmacovigilance or Drug Safety and Quality Assurance and Management System.
- Qualified Pharmacovigilance Certified (where applicable by regulatory bodies) or equivalent experience.
- Familiarity with Signal Detection and Risk Management Activities.
This is a challenging opportunity for an individual who is passionate about ensuring patient safety and product integrity.