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Pharmacovigilance and Regulatory Affairs Specialist

Ergomed · Buenos Aires

New
Mid 🇬🇧 English
Microsoft Office Word Excel PowerPoint

Job description

About the role

Ergomed is looking for a Specialist, Local Regulatory and PV network to act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA). The role is the primary local RA & PV representative ensuring compliance with national pharmacovigilance and regulatory requirements, and supports the Marketing Authorisation Holder (MAH) in keeping products compliant throughout their lifecycle.

Key responsibilities

  • Prompt and effective communication with the MAH and local regulatory authorities as required
  • Serve as the primary contact for Regulatory Affairs and Pharmacovigilance with local authorities
  • Provide local regulatory intelligence screening and expert advice for the responsible region(s)
  • Collect and report locally suspected ADRs or ICSRs (FUs, translations)
  • Manage and oversee risk minimization measures for urgent safety restrictions and emerging safety issues
  • Support the development and implementation of the local pharmacovigilance system in line with the Global MAH's system and local regulations
  • Perform local non-indexed literature screening and screen regulatory authority websites for potential ADRs and safety information
  • Maintain accurate local records and documentation, and prepare documentation for regulatory submissions
  • Provide review and linguistic input on local Product Information and mock-ups
  • Support audits and inspections, and handle local QA tasks such as suspected falsified products and quality alerts from health authorities

Required profile

  • Bachelor's degree in Life Sciences or Chemistry, Nursing or equivalent professional experience
  • At least 3 years of pharmacovigilance or safety-related experience in a pharmaceutical, CRO or regulatory environment
  • Good understanding of ICH GVP and local pharmacovigilance requirements (training or practical exposure)
  • Experience in case handling, literature screening or local PV activities preferred; prior Regulatory Affairs experience preferred but not mandatory
  • Proficiency in English; additional languages are advantageous

Required skills

  • Strong Microsoft Office skills, including Word, Excel and PowerPoint

Questions fréquentes

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Published 10 hours ago

Expires 1 month from now

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Ergomed

Buenos Aires