Manager Medical Information

  • Vor 4 Tagen veröffentlicht
  • Wien, Österreich
  • Mit Berufserfahrung
  • Feste Anstellung
  • Vollzeit
  • Hybrid
  • Homeoffice möglich

We are looking for an experienced and scientifically driven Medical Information Manager to deliver a high-quality, compliant, and insight-driven Medical Information (MI) service globally. You will oversee the global medical information management system, ensuring data integrity, regulatory compliance, and operational excellence.

Deine Aufgaben

  • Provide high-quality, evidence-based responses to medical inquiries, ensuring compliance with regulatory and legal requirements.
  • Conduct literature searches and analyze clinical data to support accurate scientific communication.
  • Develop, review, and maintain Medical Information content (Standard Responses, FAQs) within Veeva.
  • Analyze inquiry trends and generate insights for Global and Affiliate stakeholders.
  • Serve as the global escalation point for complex inquiries in collaboration with vendors and Global Medical Affairs.
  • Act as subject matter expert for compliance topics including Pharmacovigilance, Regulatory Affairs, and Data Privacy.
  • Support and optimize digital MI solutions (e.g., Veeva MedInquiry) and ensure data governance standards.
  • Deliver product, system, and process trainings to internal teams and external partners.
  • Ensure inspection readiness and adherence to SOPs, industry codes, and internal compliance standards.
  • Collaborate cross-functionally with Regulatory, PV, Legal, and Medical Affairs teams globally.

Dein Profil

  • Advanced degree in Life Sciences, Pharmacy, or Medicine
  • 5+ years of experience in Medical Information, Medical Affairs, or a related function within the pharmaceutical industry.
  • Strong scientific background with excellent analytical and medical writing skills.
  • Experience working with global teams and external vendors.
  • Familiarity with Veeva Medical Information systems (e.g., MedInquiry) is an advantage.
  • Solid understanding of regulatory, pharmacovigilance, and data privacy requirements.
  • Strong communication, presentation, and stakeholder management skills.
  • High level of accuracy, attention to detail, and compliance mindset.

Deine Benefits:

  • An open corporate culture with the opportunity to contribute your own ideas
  • Working independently in a collegial and committed team
  • Modern working environment with good public transport connections (U4 – Heiligenstadt)
  • Flexible working hours (flexitime/time-out days), bonus scheme, additional benefits and employee events
  • Structured onboarding and support through a buddy system
  • Market-oriented remuneration packages aligned with qualifications and professional experience (collective agreement minimum salary: EUR 45.080 gross per year, based on full-time employment)

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