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Medical Review Manager

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Pfizer

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Location:
Belgium , Elsene

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Category:
Pharmacy

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

The Medical Review Manager (Temporary assignment) will be a key member of the Medical Information and Review (MI&R) Group. As a key partner to in-country Medical Affairs and Marketing colleagues, this position aims to minimize compliance risks by ensuring review and approval of promotional and non-promotional marketing materials, as well as Medical to Medical content ensuring alignment with all applicable country laws, regulations, and industry codes. As an active thought leader and medical processes partner, this role will also draw upon best practices to identify new ways of working and drive continuous improvement that generates value for colleagues in-country. This vacancy is a 12 months temporary assignment. You will become part of the International Medical Review team with your focus on Belgium/ Luxembourg.

Job Responsibility:

  • Act as the point of contact for Medical Review, enabling efficient review processes for both promotional/ non-promotional and Medical-to-Medical materials
  • Identify and assess strategic opportunities for in-country service and operations improvements
  • Collaborate with cross-functional and cross-country teams to build consensus and influence decision-making
  • Acquire and maintain in-depth scientific knowledge of Pfizer medicines within nominated therapy area(s), including those in development
  • Independently perform fact-check, scientific review and medical approval of promotional and medical materials and activities in line with local product label information, country-specific code and regulatory requirements
  • Provide specialist medical, scientific and code/regulatory advice to teams during the development phase of materials/projects/activities
  • Provide advice that will ensure that the highest ethical standards are upheld, and that Pfizer always remains compliant with regulations
  • Develop and sustain constructive, continuous improvement focused relationship with leadership and stakeholders

Requirements:

  • University degree (Bs, Ms, Phd,) in pharmacy or MD (other relevant fields also considered)
  • 4-6 years of experience in medical review, compliance or related roles
  • Strong understanding of local and global regulations
  • RIP number is an advantage
  • Fluent in French with a good knowledge of Dutch OR fluent in Dutch with a good knowledge of French and fluent in English
  • Solution driven and quality oriented
  • You demonstrate ability to work independently, take ownership of tasks, and deliver results with a strong sense of accountability
  • You are self-motivated and proactive in managing responsibilities with strong organizational skills to manage multiple projects simultaneously
  • You can prioritize tasks effectively and meet deadlines consistently
  • You have proven ability to influence decisions and negotiate effectively
  • You are confident in guiding decision-making processes when necessary
  • You are a team player with a collaborative mindset, willingness to engage in cross-functional collaboration with local and global teams and you understand business dynamics and you can contribute to strategic discussions

Nice to have:

  • RIP number is an advantage
  • other languages will be considered as an advantage

Additional Information:

Job Posted:
February 20, 2026

Expiration:
February 25, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
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