ROLE SUMMARY:

Medical Affairs Review and Approval (MARA) team은 promotional material (판촉물) 및 의약품 광고를 리뷰 및 승인하는 것을 전담하는 팀입니다.

MARA expert 는 사업부에서 개발하는 판촉물 및 의약품 광고가 약사법 및 관련 규정, 내부 policy에 맞게 제작되었는지 리뷰하고 승인하는 것을 주요 업무로 하고 있습니다. 또한, 사업부에서 계획하는 brand plan 에 대한 contribution 및 더 적절한 리뷰 process를 지속적으로 개선하고 수립하는데 기여하게 됩니다.

The Medical Affairs Review and Approval Expert (MARA) is the Medical expert responsible for the medical review and approval of all promotional and non-promotional materials across BU’s in accordance with market regulations and company policies.

The MARA actively provides scientific expertise and support to cross-functional teams in executing strategies and plans in support of their product portfolios. The MARA is a key contributor to the development of brand plans and in the adjudication process, associated with complaints/defence against complaints regarding promotional claims.

ROLE RESPONSIBILITIES:

• Review and/ or approval of promotional/ non-promotional materials across BUs in compliance with local regulations and global/ local procedures thru the relevant systems (MLR review & approval in GCMA)

• Ensure scientific accuracy of claims, references & translations and ensure alignment with local product label.

• Contribute to ensure local content promotional compliance

• Collaborate closely with the relevant cross functional colleagues across BUs to ensure a streamlined approach

• Collaborate closely with Medical Affairs and commercial and content generation stakeholders

• Meaningfully contribute to cross-functional teams in: 1. the development of promotional materials at various stages of development. 2. formulating the response to any code complaints or formulation of complaints against competitors. 3. the development brand plans and PoA meetings as appropriate

• Serves as the subject matter expert for adherence of promotional content with local laws and industry codes as applicable.

• Provides input into development of relevant policies, SOPs and Work Instructions.

• Serves as a principal contact for audit and inspection teams in relation to compliance of promotional materials with applicable regulations, codes and company policies.

• Contribute to new innovative solutions to improve scientific content review and approval process and to resolve problems based on comprehensive business & scientific knowledge

• Actively 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:

• 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 & 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

Application Deadline: August 16 (Tues), 2022 6:00 pm

Please apply via Pfizer Career Website Only.

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