Pharmacovigilance Specialist (Case Processing / Mandarin language)

Key Responsibilities:

• Manage and process end-to-end safety case reports in compliance with global and local regulatory requirements
• Perform triage of incoming safety information, assessing case validity, seriousness, and required follow-up actions
• Review, manage, and archive source documentation in accordance with pharmacovigilance regulations and internal SOPs
• Perform safety database (SDB) data entry, including narrative writing and case documentation
• Conduct medical assessments, including seriousness, causality, and expectedness evaluations
• Assess reporting requirements and ensure timely submission to health authorities and clients
• Perform and document follow-up activities and manage safety-related queries
• Execute quality control checks to ensure data accuracy, completeness, and compliance
• Perform reconciliation activities to ensure consistency across safety databases and source documents
• Prepare line listings and safety reports as required by projects or clients

Requirements

• Bachelor’s degree in Life Sciences field
• Minimum 1 year of experience in pharmacovigilance or safety case processing within the pharmaceutical or CRO industry
• Fluency in Mandarin Chinese (Simplified Chinese) and English, with the ability to process pharmacovigilance safety cases originating in Mandarin, is required
• Hands-on experience with Argus Safety, Veeva Vault or similar safety databases is preferred
• Strong proficiency in MS Office applications
• Ability to work independently while managing multiple cases and deadlines
• Candidates may be based in or outside China; those located in Europe or other regions and willing to work in European working hours are welcome

Benefits

• International team and environment
• Remote/home-based position