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. Build effective medical advisor interface and provide professional medical training to support commercial teams to achieve their objectives.

Lead and develop product life-cycle management strategy from medical perspective to maximize product’s value and long term development.

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) studyReview and endorse Investigator Initiate research proposal to ensure its scientific standard and strategy fitDevelop 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.Coach and guide the team to provide medical input to MI team on LSRDCoach the team to communicate medical update to internal and external customer and answer complicated medical queries.

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

Coach and guide team to design/conduct effective training programs on field force supporting programs to develop sale team’s medical capability, and solve key medical issues. 

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

Guide team to set up top national level KOL database, and effective medical communication plan through various approaches , and ensure its implementationEstablish 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 progressCoach and guide the team to provide medical support to China clinical practice  guideline development, scientific interpretation and promotion

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

Coach and develop team to perform medical evaluation, explanation on the eventApprove 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

Coach the team to provide professional medical consultation to Safety Officer to solve Pfizer products’ safety queryIf 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

TechnicalTherapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic areaLanguage: Proficiency in oral and written EnglishGood understanding about pharmaceutical businessIn-depth Clinical trial knowledgeComputer: Good at Microsoft Office softwareStrong business acumenCapability of strategic insight to drive new business direction from medical perspectiveCross functional leadership skillStrong communication and influencing skillManagerialSustain Focus on PerformanceCreate an Inclusive EnvironmentEncourage Open Discussion and DebateManage ChangeAlign Across PfizerCertifications

N/A

Education  Master degree major in clinical medicine, Medical doctoral degree or PHD in medical is preferred  Master of Business Administration is a plusExperience3 years clinical practice in Tier 3 hospitals (corresponding specially is preferred) MD or PHD with 8+ years medical affairs experience in multinational pharmaceutical companies experience, or3+ years Management experience

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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