Position Purpose

Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. In this position, you will:

provide leadership to dedicated medical affairs teambe responsible for development of the Medical Plan and Strategy for oncologybe a member of the Country Medical and the Oncology Commercial Leadership Teamensure compliance of medical team with country Code of Practice and relevant procedures, regulations and guidelineswork closely with internal and key external stakeholders supporting Pfizer strategy and bringing medical insights as well as support for media, government and patient group activities, including policy development, corporate initiatives and issues managementtake accountability for reviewing and certificating promotional and non-Promotional materialsgive input into HEOR submissions, HTA dossiers, clinical guideline consultations and regional formulariesclosely collaborate with Development Japan by providing input on development and regulatory strategiessupport for issues related to supply and distribution, product quality, benefit-risk, market actions and product withdrawals

Responsibility

Leadership of medical team, including setting business objectives, performance management and team developmentResponsibility for development of the Medical Plan/Strategy for relevant therapeutic areasRecruitment, development and retention of talented colleague• Coaching and guidance of colleagues to support them achieving their maximal potentialMembership of Medical and Commercial Leadership TeamsResource allocation to ensure appropriate resources to fulfil medical objectives and business needsEnsure compliance of medical team with country Code of Practice and relevant SOPs, regulations and guidelinesCollaboration with internal stakeholders to ensure timely receipt of information on brand strategy, clinical plan, new clinical data, new regulatory and safety information and accurate, balanced and up to date materials to use in medical to medical communicationsWork with key external stakeholders during the life-cycle of Pfizer medicines, supporting Pfizer strategy and bringing external insights to the organisation to shape strategy and providing focused, relevant information in response to their needsReview and certification of promotional and non-promotional materials and activities and approval of customer engagement programsEnsure that product materials and related activities reflect the most up to date regulatory labelling and risk management plans and regulatory commitments• Input into regulatory submissions, clinical overviews, license variations and CDS updates as required• Input into HEOR submissions, HTA dossiers, clinical guideline consultations and regional formularies as requiredInput into assessment and due diligence of business development initiatives• Support for issues related to supply and distribution, product quality, benefit-risk, market actions and product withdrawals related to portfolioSupport for in country clinical research programs, including protocol and site feasibilities related to portfolioProtocol approval and oversight of in country non-interventional studies related to portfolioSupport for investigator sponsored research (ISR) studies to ensure that appropriate records are kept and progress is monitoredSupport for media, government and patient group activities, including policy development, corporate initiatives and issues managementParticipate in local, regional and global cross-functional project teams to ensure that ongoing improvements in processes and performance are deliveredAccountable for medical team IIR and headcount/expenses budgetsRepresent the country and countries interests to European and Global teams

Desired Skill Set

 MD / Ph.D with knowledge in oncologySignificant pharmaceutical industry experience (oncology preferable) and excellent understanding of the local healthcare environmentQualifications to act as in country signature, or have qualifications and potential to become a medical signatory is mandatoryExcellent communication and presentation skills both in English and JapaneseGood knowledge of pharmaco-vigilance and regulatory legislation and how it impacts the product portfolioGood knowledge of drug developmentStrong people management and leadership skills and excellent business acumenAbility to prioritize resources in line with brand and customer strategyTeam playerHigh degree of cross-functional leadership and collaborationCommunication and influencing skillsRole modelling, upholding values, adhering to standards, visibility Leadership skillsFluent language skills in Japanese and English

Organizational Relationships

You will collaborate closely with Medical Leads in other therapeutic areas and ONC commercial leadership team as well as the relevant platform functions such as Regulatory Affairs, Drug Safety, MQO, Medical Operation, Medical Information, Medical Grant Management, Compliance, Legal and Product quality to ensure adequate external representation.

 
 

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

Medical

#LI-PFE