Pharmacovigilance (Case Processing) Specialist (Mandarin language)

AI overview

The role focuses on end-to-end pharmacovigilance case processing, including safety assessments and regulatory compliance, while working with a global team.

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.

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

Perks & Benefits Extracted with AI

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

Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle. Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.

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