• Evaluate new products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support new product introduction and line extension
• Align with cross function team including marketing, CCO team, global team etc, develop post marketing research strategy based on Registration/Market needs
• Provide phase IV study direction and develop key elements
• Design and manage local Non-interventional Study (NIS) study as a clinician.
• Develop medical strategy and implement it to support product development
• Develop publication plan and implement it
• Evaluate and review Investigator Initiate research proposal to ensure its scientific standard and strategy fit

• Co-develop product strategy, positioning, key message with Marketing team
• Provide medical support (topic design, KOL communication etc.) on key marketing activities
• Provide broad and deep medical insight/summary document of the defined therapeutic area to business partners to deal with key product issues such as bidding, RDL, new initiatives etc.
• Review and approve Local Standard Response Letter to HCPs

• At Phase I sales training
• At National sales conference
• Field visit
• Special sales force program
• Give lectures or updates to other stakeholders to increase their disease and product knowledge

• Timely review and approval of local product labeling (LPD)
• Develop medical justification document to support LPD related queries from government
• Provide medical input in feasibility evaluation of studies for global trials
• Provide official input on study site selection from therapeutic prospective
• Provide input to registration protocol synopsis and study report as necessary

• Set up national level KOL database, and keep medical communication with through various approaches
• Design educational programs for top KOLs and implement them
• Support on China treatment guideline development, scientific interpretation and promotion
• Publish or facilitate publication of medical paper in professional journals
• Cooperation with local medical societies to conduct medical programs/conference to facilitate new concept and state of art medical progress’ introduction to China

• Perform medical evaluation, explanation on the event;
• Develop medical justification or responding document.
• Provide medical expert opinion on company responding strategy
• Review and approve all external communication documents to make sure all delivered message are medically precise and consistent
• Communicate with external customers directly for medical issues as necessary

• Provide professional medical consultation to Safety Officer to solve Pfizer products’ safety query
• If 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 Safety Review Plan (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, theclinical 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 SAF09 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.

• Act as the sole reviewer to ensure educational grants within medical compliance

• Review and approve promotional materials and activities to ensure their scientific standard and medical compliance with external and internal requirements

• Technical

• Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area
• Language: Fluent in English (both spoken and written) is preferred
• Primary Clinical trial knowledge
• Computer: Familiar with Microsoft Office software is preferred
• Ability to rapidly catch up global leading edge medical advancement
• Strong business acumen
• Strategic thinking and analytic skills
• Good interpersonal communication skills
• Proactive planning and result oriented
• Customer focus
• Excellent Teamwork/Collaboration

• Managerial

• Sustain Focus on Performance
• Accountability
• Manage Change
• Align Across Pfizer

• Education

• Clinical Medicine Background in the defined therapeutic area, master degree, Master above is required

• Minimum 3+years of experience of clinical practice in Tier 3 hospitals is preferred
• Preferred experience as Medical Advisor or MSL in other multinational pharmaceutical companies.

Medical #LI-PFE