ROLE SUMMARY

Expectations for Senior Medical Reviewer include, but are not limited to, reviewing promotional materials and medical content in accordance with market regulations and company policies. The Senior Medical Reviewer provides scientific expertise and support to cross-functional teams in executing strategies and plans in support of their product portfolios. The Senior Medical Reviewer is a contributor to the development of brand plans and in the adjudication process, associated with complaints/defense against complaints regarding promotional claims.

Senior Medical Reviewer는 의약품 광고 및 메디컬 컨텐츠의 리뷰 및 승인을 전담하는 팀에 속하여 사업부 또는 의학부에서 개발하는 의약품 광고와 메디컬 컨텐츠가 약사법 및 관련 내/외부 규정에 맞게 제작되었는지 리뷰하고 승인하는 것을 주요 업무로 하고 있습니다.  

ROLE RESPONSIBILITIES

• Serves as the subject matter expert for adherence of promotional and medical content with local laws and industry codes as applicable.
• Reviews materials in compliance with applicable SOPs and work instructions.
• Ensures the scientific claim is fully substantiated by the cited references.
• Meaningfully contribute to cross-functional teams in:
  • the development of promotional materials at various stages of development
  • formulating the response to any code complaints or formulation of complaints against competitors
  • the development brand plans and PoA meetings as appropriate
• Serves as a principal contact for audit and inspection teams in relation to compliance of promotional materials and medical content with applicable regulations, codes and company policies. Provides input into development of relevant policies, SOPs and Work Instructions.
• Actively contribute to new innovative solutions to improve scientific content review and approval process and to resolve problems based on comprehensive business & scientific knowledge
• Actively participates or leads/co-leads local and/or global projects that have an impact beyond the function and/or the country
• Contribute to mentoring, coaching and training of new and existing colleagues within the team.  
• Contribute to resolving issues related to the day-to-day work, proposes recommendations and drives implementation of required changes, new processes, etc.
• Contribute to strategic partnerships with relevant cross-functional teams with a view to sustaining, and identifying new ways for Medical to add value to the Pfizer business

 QUALIFICATIONS

 Technical:

• Major in medicine, pharmacy or science with an appropriate life science major preferred. Degrees from other relevant disciplines also considered.
• More than 2 years’ experience in the pharmaceutical industry in a Medical Information, Medical Affairs or related function.
• Well versed in reviewing promotional materials and medical content & the promotional complaints process.
• Demonstrates excellent collaboration, interpersonal & relationship management skills with ability to influence and negotiate outcomes. Experience working in cross-functional teams highly preferred
• Ability to work in a virtual work environment
• Proficient at critically evaluating literature and writing/summarizing clinical and scientific data
• Exhibits strong analytical, oral and written communication skills
• Able to work in a fast-paced environment with competing priorities and tight deadlines
• Effectively deals with ambiguity and adapts quickly to change
• Demonstrates initiative and works independently on complex projects
• Fluency in English preferred

Education:

• Major in medicine, pharmacy or science with an appropriate life science major preferred. Degrees from other relevant disciplines also considered.

Experience:

• More than 2 years’ experience in the pharmaceutical industry in a Medical Information, Medical Affairs or related function.

Application Deadline: 6pm, 20th, March 2025.

 Work Location Assignment: On Premise
 

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

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