Medical Information and Review Scientist

Pfizer Pfizer · Pharma · Estonia, Lithuania

This role focuses on providing medical information and reviewing marketing materials for Pfizer products, with an emphasis on using approved AI tools and identifying AI-enabled opportunities to improve efficiency and consistency in medical information and review activities. The role is customer-facing and requires adherence to regulatory and compliance standards.

What you'd actually do

  1. MI frontline and digital Customer Experience activities to provides technical and medical information to HCP and patients/caregivers with high a degree of quality and customer service in the local language.
  2. In addition, the responsibilities include medical review and approval of promotional and non-promotional marketing materials as well as Medical to Medical content in line with local product label information and applicable country law, industry code and regulatory requirements.
  3. Demonstrate AI fluency by appropriately using approved AI tools and systems for identified used-cases, implement AI-based innovations in alignment to organizational vision and compliance with Pfizer policies.
  4. Identify, evaluate, and support AI-enabled opportunities to enhance efficiency, quality, and consistency across Medical Information & Review activities, including content development, insights generation, and operational processes.
  5. Contribute to AI adoption and capability building by sharing learnings, best practices, and practical use-cases with colleagues to promote responsible, value‑driven AI utilization within the organization.

Skills

Required

  • Medical information provision
  • Medical review of promotional and non-promotional materials
  • Scientific accuracy validation
  • Compliance with local regulations and industry codes
  • Customer service
  • Documentation and record-keeping
  • Adverse event and product quality complaint reporting
  • Use of approved AI tools and systems
  • Identification of AI-enabled opportunities
  • Communication of AI learnings and best practices

Nice to have

  • Second-line escalation support
  • Content management
  • Therapeutic area expertise
  • Liaison with health authorities
  • Project management

What the JD emphasized

  • fixed term period of 18 months
  • customer-focused group
  • unsolicited medical inquiries
  • reviewing, analyzing, and validating promotional, non-promotional, and other content for scientific accuracy and compliance
  • local product label information and applicable country law, industry code and regulatory requirements
  • adverse events and product quality complaints
  • fact-check, scientific review and medical approval
  • compliance with local code/regulations
  • approved AI tools and systems
  • AI-based innovations
  • AI-enabled opportunities
  • responsible, value‑driven AI utilization