Pharmacovigilance Specialist (Case Processing / Mandarin language)
Biomapas
Apply to this jobBiomapas & 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.
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
- Monthly bonuses
Summary
Manage safety case reports, perform medical assessments, ensure compliance, and document pharmacovigilance activities
Job title
Pharmacovigilance Specialist (Case Processing / Mandarin language)
Experience level
1+ years
Industry
pharmaceutical
Location requirements
remote work allowed, based in China or outside
Salary
Not specified
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
China