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French speaking Affiliate Pharmacovigilance QC Associate

Position Overview:We are seeking a French-speaking Affiliate Pharmacovigilance QC Associate for a full-time role based in Budapest, Hungary. This position offers a hybrid work mode, requiring office attendance once per week.
What We Offer:

  • Competitive salary and benefits package, including cafeteria and annual bonus
  • Opportunities for training, continuous learning, and certification
  • A chance to be part of a rapidly expanding organization
  • A multilingual, multicultural environment with native colleagues
  • Discounted All You Can Move SportPass
  • Free medical benefit package
  • Reimbursable language courses
  • Team and company events
  • Relocation package
  • High-value awards and recognitions


Your Profile:

  • Graduate in Pharmacy or Life Science
  • At least 1 year of pharmacovigilance or relevant clinical experience
  • Excellent proficiency in spoken and written French and English


Responsibilities:

  • Receive and download information from various channels and handle voice calls for reporting safety information
  • Route information and safety reports to the appropriate departments
  • Monitor mailbox, triage patient safety reports and emails
  • Maintain and archive emails/source documents and update shared folders
  • Handle source documents and enter data into the front-end system as per triage criteria
  • Obtain consent from reporters to follow up on safety reports
  • Assess cases for missing information and follow up until closure
  • Check case validity and perform initial checks to prevent duplicate entries
  • Ensure clarification requests in case of data discrepancies
  • Enter safety information into the system and evaluate for case seriousness
  • Translate and back-translate safety information as needed
  • Review and archive source data records for any missing or discrepant safety information
  • Identify discrepancies and maintain email clarifications for SDV
  • Extract and process Individual Case Safety Reports from Health Authority databases/registries
  • Document review processes and ensure completion of day-to-day work within agreed SLAs
  • Maintain data as per customer guidelines
  • Collaborate with project quality roles to improve case quality
  • Attend training sessions and develop skills continuously
  • Coordinate with internal teams for necessary information
  • Assist in training and mentoring new joiners as needed

French speaking Affiliate Pharmacovigilance QC Associate

Budapest
Full time

Published on 19.07.2025

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