Biomapas

Pharmacovigilance Specialist (Case Processing)

🇵🇱 Віддалено, Польща Віддалено Охорона здоров'я та наука Повна зайнятість Середній рівень Опубліковано Чер 5, 2026
Локація Віддалено, Польща
Формат роботи Віддалено
Тип зайнятості Повна зайнятість
Рівень досвіду Середній рівень
Мова English
Опубліковано 05 червня 2026 р.
Остання перевірка 08 червня 2026 р.
Контекст JobGrid

Огляд ролі від JobGrid

Pharmacovigilance Specialist (Case Processing) at Biomapas is a mid-level, full-time remote role in Poland, classified by JobGrid under Healthcare & Science. JobGrid keeps the role facts normalized for comparison, notes the English-language CV requirement from the source posting, and sends candidates to the original public application page with non-personal referral parameters.

  • Remote, Poland; full-time; mid-level; Healthcare & Science.
  • Focus areas include safety case reporting, case processing, and literature screening.
  • Source posting was last checked on 2026-06-08, so the page reflects recent source verification.
  • The application path leads to the original employer page through JobGrid's referral flow.

The Pharmacovigilance Specialist will be responsible for ensuring the operational delivery of assigned tasks at the project level, with a focus on safety case reporting, processing of safety case report data, and literature screening activities. The role involves communication with the Pharmacovigilance Team Leader and Pharmacovigilance Manager regarding potential risks related to operational delivery, quality standards, client relationships, and the company's reputation, as well as addressing ad hoc project tasks and requirements.

CV must be in English language for further assessment.

Position is full-time remote/home-based in any EU country.

Responsibilities:

  • Oversee and manage the workflow of safety case reports, ensuring efficient processing
  • Perform triage on safety case reports to assess priority and necessary actions
  • Review, manage, and file source documentation in compliance with regulatory requirements
  • Process safety case reports, including SDB data entry, narrative writing, seriousness assessment, medical review (including causality and expectedness assessments), and reporting requirements evaluation
  • Conduct follow-up activities and manage queries related to safety case reports
  • Execute quality control checks on data entry and case processing to ensure accuracy and compliance
  • Reconcile safety case reports to ensure consistency and completeness of data
  • Prepare line listings to summarize and report on safety case data