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Pharmacovigilance Specialist; Case Processing/Mandarin language
Remote / Online - Candidates ideally in
Greater London, London, Greater London, W1B, England, UK
Listed on 2026-01-31
Greater London, London, Greater London, W1B, England, UK
Listing for:
Biomapas
Remote/Work from Home
position Listed on 2026-01-31
Job specializations:
-
Healthcare
Clinical Research
Job Description & How to Apply Below
Location: Greater London
Overview
Biomapas & Delta PV looking for a Pharmacovigilance (Case Processing) Specialist with Mandarin language.
Pharmacovigilance Specialist will be responsible for the operational delivery of pharmacovigilance activities at the project level, with a primary focus on safety case intake, processing, and reporting. The role involves end-to-end case processing rather than translation, including medical assessment and regulatory compliance activities.
- 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
- 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
- International team and environment
- Remote/home-based position
- Monthly bonuses
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