Pharmacovigilance; Case Processing Specialist; Mandarin language
Position: Pharmacovigilance (Case Processing) Specialist (Mandarin language)
Location: Town of Italy
Overview
Biomapas & Delta PV are 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.
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
Qualifications
• 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
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Apply Now
Apply Now
Location: Town of Italy
Overview
Biomapas & Delta PV are 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.
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
Qualifications
• 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
#J-18808-Ljbffr
Apply Now
Apply Now