? 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. o
Develop and execute medical plan for the defined therapeutic area(s) aligning
with products development strategy o Identify 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
decisions o Evaluate new products, new indications, new research programs, new
business potentials of defined therapeutic areas from medical perspective to
support business decisions o Develop post marketing research strategy based on
registration/market needs in alignment with cross function team including
marketing, CCO team, and global team o Evaluate and endorse phase IV study
direction, and drive its endorsement from company o Oversee and manage local
Non-interventional Study (NIS) study o Review and endorse Investigator Initiate
research proposal to ensure its scientific standard and strategy fit o 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 accuracy o Work with
BU marketing and sale leaders on therapeutic strategies and key issues
resolution from medical point of view o Review and approve medical dossier for
drug reimbursement listing, pricing bidding and other access related issues. o
Coach and guide the team to provide medical input to MI team on LSRD o Coach
the team to communicate medical update to internal and external customer and
answer complicated medical queries. Develop sale team medical capability
through medical training ,lecture delivery and medical knowledge update through
various channel o 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 o Provide medical advice to registration trials protocol synopsis
and study report o Review and approve of local product labeling (LPD) o Review
and approve medical justification document to support LPD related queries from
drug administration agency o Provide medical input in feasibility evaluation of
global and local trials o Provide 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 o Guide
team to set up top national level KOL database, and effective medical
communication plan through various approaches , and ensure its implementation o
Establish strategic partnership with local medical association through
appropriate medical programs o Cooperate with local medical association to
facilitate new concept and the state of the art medical progress o Coach 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 o Coach and develop team to perform medical
evaluation, explanation on the event o Approve medical responding document o
Provide medical expert opinion and guidance on company responding strategy o
Review and approve all external communication documents to make sure all
delivered message are medically precise and consistent o Communicate with
external customers directly for medical issues as necessary Provide medical
expert opinion in safety events management to avoid negative impact o Coach the
team to provide professional medical consultation to Safety Officer to solve
Pfizer products’ safety query o 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) o 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 o Act as the sole reviewer to ensure educational
grants within medical compliance o Review and approve promotional materials and
activities to ensure their scientific standard and medical compliance with
external and internal requirements.