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BiomapasBI

Pharmacovigilance (Case Processing) Specialist (Mandarin language)

Biomapas is a functional and full outsourcing solution provider to the global life science industry, with key expertise in Clinical Trials, Regulatory Affairs, Pharmacovigilance, and Medical Information.

Biomapas

Employee count: 201-500

China only

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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

About the job

Apply before

Posted on

Job type

Full Time

Experience level

Education

Bachelor degree

Experience

1 year minimum

Location requirements

Hiring timezones

China +/- 0 hours

About Biomapas

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Biomapas embarked on its journey in 2001, establishing its roots in Lithuania with a clear vision: to become a pivotal partner for the global life science industry. What began as a focused endeavor to provide clinical research services in the Baltics quickly evolved. By 2002, the company launched its Phase I-IV clinical research services, marking its formal entry into supporting drug development. The subsequent year, 2003, saw Biomapas conduct its first clinical trial in Belarus, signaling an early ambition for broader regional engagement. This expansion continued, and by 2004, Biomapas was already involved in clinical trials with biological and biosimilar products, showcasing its adaptability to the evolving pharmaceutical landscape.

The company's service portfolio broadened significantly in 2005 with the introduction of full-scope pharmacovigilance services, a critical component in ensuring drug safety post-market. Recognizing the increasing complexity of drug approval processes, Biomapas launched its regulatory affairs services in 2009, further solidifying its role as a comprehensive solutions provider. A commitment to quality and standardized processes was underscored in 2012 with the achievement of ISO 9001:2008 certification. Over the years, Biomapas has consistently expanded its geographical reach and service capabilities, now operating in over 60 countries across Europe, the CIS region, MENA, and EAEU. This growth has been driven by a dedication to combining global standards with local expertise, leveraging technology for efficiency, and fostering senior-level partnerships. Today, Biomapas stands as a functional and full outsourcing solution provider, offering expertise in clinical trials, regulatory affairs, pharmacovigilance, and medical information, always aiming to advance clinical development and ultimately improve patient health worldwide.

Employee benefits

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Competitive salary and benefits

Offers competitive salary and benefits.

Work-life balance initiatives

Many initiatives that will make your daily office life comfortable and support work-life balance.

International environment

Colleagues from more than 15 countries allow us to develop ourselves professionally and personally.

Professional and personal development

Guarantee for professional and personal development, including Biomapas academy and Leadership academy.

View Biomapas's employee benefits
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Biomapas

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