
Pharmacovigilance Specialist
2 days ago
Job Responsibility:
- Adverse Event Case Processing:
Reviewing, evaluating, and processing individual case safety reports (ICSRs) to ensure accurate and timely reporting to regulatory authorities.
- Regulatory Compliance:Maintaining up-to-date knowledge of global pharmacovigilance regulations and guidelines, ensuring compliance with reporting timelines and requirements.
- Safety Database Management:Maintaining and updating pharmacovigilance databases, ensuring data quality and integrity.
- Signal Detection and Management:Participating in activities related to signal detection and management, including data analysis and evaluation of potential safety signals.
- Stakeholder Communication:Interacting with healthcare professionals, patients, and other stakeholders to address safety-related inquiries and provide information.
- Report Writing:Preparing and reviewing various safety reports, including aggregate reports (e.g., periodic safety update reports) and regulatory submissions.
- Quality Control:Ensuring the quality and accuracy of all pharmacovigilance activities, including data management and report writing.
Qualifications:
- BS Pharmacy Graduate with or without license
- No experience required, fresh graduates are welcome to apply
- Deep understanding with drug related terminologies
- Must be amenable to work night shifts
- Must me amenblt to work onsite in Taguig City
Job Types: Full-time, Permanent
Pay: Php25, Php30,000.00 per month
Benefits:
- Additional leave
- Company Christmas gift
- Company events
- Health insurance
- Opportunities for promotion
- Paid training
- Pay raise
- Promotion to permanent employee
Work Location: In person
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