Maximize the value of Pfizer products to Chinese patients and health care professional within Pfizer’s vision and mission. Develop China medical development and life-cycle management strategy for inline products and pipeline within Pfizer China business objectives and strategy. Provide state of the art medical and clinical development expertise to drive Pfizer clinical trials. Establish platform and channel with China academic organization in defined therapeutic area to delivery Pfizer products message to key influencers and stakeholders. Lead the conversation interally and externally in Pfizer products related therapeutic area. Build effective medical advisor interface and provide professional medical training to support commercial teams to achieve their objectives.

Develop and execute medical plan for the defined therapeutic area(s) aligning with products development strategy independently

Develop and execute medical plan for the defined therapeutic area(s) aligning with products development strategyIdentify medical opportunity in current trends of diagnosis, existing/emerging treatment options , and unmet medical needs in defined therapeutic area as medical base for business initiative and decisionsEvaluate new products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support business decisionsDevelop post marketing research strategy based on registration/market needs in alignment with cross function team including marketing, CCO team, and global teamEvaluate and endorse phase IV study direction, and drive its endorsement from companyOversee and manage local Non-interventional Study (NIS) study

Support investigator sponsored research, ensure its scientific standard and strategy fit

Develop and execute publication plan, provide input to the publication plan, provide ideas for generating manuscripts of scientific interest, and actively review manuscripts and abstracts to ensure medical and scientific accuracyWork with BU marketing and sale leaders on therapeutic strategies and key issues resolution from medical point of viewReview and approve medical dossier for drug reimbursement listing, pricing bidding and other access related issues.Lead and collaborate with other medical members to provide medical input to relevant cross-functional teams (including MI team, MA team, etc), set an example to the team and assist the managerEffectively communicate with internal and external customers and answer medical queries, set an example to the team and assist the manager

Develop sale team medical capability through medical training, lecture delivery and medical knowledge update through various channel

Design/Conduct effective training programs to develop sale team’s medical capability, and solve key medical issues, , set an example to the team and assist the manager

Support products registration activities

Provide medical advice to registration trials protocol synopsis and study reportReview and approve of local product labeling (LPD)Review and approve medical justification document to support LPD related queries from drug administration agencyProvide medical input in feasibility evaluation of global and local trialsProvide official input on study site selection from therapeutic prospective

Enhance the delivery of new concept and Pfizer products key message to key influencers /stakeholders, and establish cooperation and partnership with medical association to promote medical advancement

Lead and cooperate with cross-functional teams to set up top level KOL database, and effective medical communication plan through various approaches, and ensure its implementation, analysis,  and evaluation. Set an example to the team and assist the managerEstablish strategic partnership with local medical association through appropriate medical programsCooperate with local medical association to facilitate new concept and the state of the art medical progressProvide medical support to China clinical practice guideline development, scientific interpretation and promotion, set an example to the team and assist the manager

Act as a core member to work with cross function team on crisis management to maintain company’s image and protect patient’s welfare

Perform medical evaluation, explanation on the event, set an example to the team and assist the managerApprove medical responding documentProvide medical expert opinion and guidance on company responding strategyReview and approve all external communication documents to make sure all delivered message are medically precise and consistentCommunicate with external customers directly for medical issues as necessary

Provide medical expert opinion in safety events management to avoid negative impact

Provide professional medical consultation to Safety Officer to solve Pfizer products’ safety query, set an example to the team and assist the managerIf take clinician role: provide the clinical safety oversight including performing and documenting; regular review of individual subject safety data and performing review of cumulative safety data with the safety risk lead (as delegated by the clinical lead)If take clinical lead role: consistent with SRP, performs and documents regular review of individual subject safety data, and performs review of cumulative safety data with the safety risk lead. As appropriate, the clinical lead may delegate these responsibilities to the study clinician identified in the SRP. The specific components of safety data review are detailed in the Safety Data Review Guide – for Clinicians and in SAF 09 SOP. For all studies, clinical safety review should be performed in consultation with a designated medical monitor if neither clinical lead nor clinicians are medically qualified.

Ensure company’s medical compliance

Act as the sole reviewer to ensure educational grants within medical complianceReview and approve promotional materials and activities to ensure their scientific standard and medical compliance with external and internal requirements

REQUIRED SKILL SET

•       Technical

Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic areaLanguage: Proficiency in oral and written English Good understanding about pharmaceutical business In-depth Clinical trial knowledgeComputer: Good at Microsoft Office softwareStrong business acumen Capability of strategic insight to drive new business direction from medical perspectiveCross functional leadership skillStrong communication and influencing skill

•      Managerial

Sustain Focus on PerformanceCreate an Inclusive EnvironmentEncourage Open Discussion and DebateManage ChangeAlign Across Pfizer

•       Certifications

N/A

•       Education

Master degree major in clinical medicine, Master above in the defined therapeutic area is preferred.

•       Experience

3 years clinical practice in Tier 3 hospitals (corresponding specially is preferred)  MD or PHD with 3+ years medical affairs experience in multinational pharmaceutical companies’ experience, or Master with 5+ years’ experience 
 

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

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