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Pharmacovigilance Associate Germany

Biomapas
Remote
Posted about 1 month ago

AI summary

As a Pharmacovigilance Associate, you will perform routine pharmacovigilance tasks such as case intake, data entry, and literature monitoring while supporting Local Safety Officers in the DACH region. You will also assist with quality control and administrative tasks related to pharmacovigilance systems.

Eligible from: Germany

Job Description

Join our global team as a Pharmacovigilance Associate in Germany.

Pharmacovigilance Associate performs routine PV tasks such as case intake, data entry, literature monitoring, and documentation management to support Local safety officers in the DACH region to maintain compliant PV operations, with further opportunity to be nominated as Local Safety Officer.

Position is remote/home-based in Germany.

All CVs must be submitted in the English language for consideration.

Responsibilities:

  • Perform routine and foundational PV activities for assigned projects (e.g., case intake, data entry, coding, literature monitoring, distribution of safety information)
  • Perform initial case intake and triage according to SOPs
  • Enter and code cases in safety databases with supervision
  • Assist in follow-up activities (requests, tracking, documenting)
  • Prepare cases for quality control review and correct findings promptly
  • End to end case processing steps under supervision
  • Assist with administrative tasks related to PV systems, including preparing files, templates, and checklists
  • Provide administrative support for audits/inspections
  • Conduct weekly literature searches using predefined search strategies
  • Document search results, identify potential safety cases, and escalate to upper level for assessment
  • Preparation of data for Aggregate Safety Reports (PSURs/PBRERs), RMP/SMP sections, and risk minimization activities

Requirements

  • University degree (or final year student) in Life Sciences or a related field
  • Fluent written and verbal English and German language
  • Foundational knowledge of pharmacovigilance principles and relevant regulatory frameworks
  • Ability to perform routine PV tasks (case intake, data entry, literature review) accurately under supervision
  • Good computer literacy and ability to learn safety databases and PV systems
  • Good organizational skills and ability to manage a routine workload effectively
  • Strong attention to detail and accuracy in documentation

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About the job

Posted on
Aug 18, 2026
Job type
Full-time
Location
GermanyRemote

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