Safety Data Management Specialist With French, German or Dutch

Pfizer Pfizer · Pharma · Warsaw, Poland

This role focuses on managing and processing safety data within the biopharmaceutical industry, ensuring accuracy, consistency, and compliance with regulatory requirements. It involves reviewing, documenting, and verifying case-related information, liaising with stakeholders, and reporting to a manager. While the company mentions digital transformation and AI/ML in drug discovery, this specific role is centered on traditional data management and pharmacovigilance processes.

What you'd actually do

  1. Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency.
  2. Process cases based on these assessments.
  3. Review case criteria to determine the appropriate workflow for case processing
  4. Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately.
  5. Write and edit case narrative.

Skills

Required

  • Fluency in English
  • Fluency in French, German, or Dutch
  • Master Degree
  • Ability to make basic decisions
  • Ability to work under supervision

Nice to have

  • Experience in pharmacovigilance
  • Experience in data management
  • Experience and skill with medical writing
  • Experience in use and management of relational databases

What the JD emphasized

  • Fluency in spoken and written: English and additional languages: French, German or Dutch