To advise and manage medical related activities in all operations of company
with medical expertise and company policies, with the objective of ensuring the
scientific validity and the ethics of operations.
Enhance local data generation and Product life-cycle management from medical
perspective to maximize product’s value and long term development
* 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
As a key partner to provide medical input on business decision making
* 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
Develop sale force’s medical capability through training program design,
Lecture Delivery and periodic medical knowledge update in different settings
through various channel
* 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
Support Drug Registration Activities
* 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
Academic communication to enhance the delivery of new concept and Pfizer
products key message to key influencers and stakeholders, and Establish
Cooperation and partnership with medical association to promote medical
advancement.
* 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
In order to maintain company’s image and protect patient’s welfare, MA act as
a core member to work with cross function team on crisis management.
* 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 medical expert opinion in safety events management to avoid negative
impact.
* 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, 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 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.
Ensure company’s medical compliance.
* 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


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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