宜昌招聘

Responsibilities
● responsible for developing 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 expertise to assist business decision.
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, ensure the
scientific validity and medical compliance of company activities. PBG>Medical>
Emerging Markets>China N
Why Patients Need You
Field-based medical colleagues provide therapeutic area /product expertise to
health care providers. You will think big and demonstrate every day that we're
a patient-centric company by looking to improve health outcomes for patients.
What You Will Achieve
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.
How You Will Achieve It
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
02As 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
02Develop 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
02Support 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
02Academic 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 approaches02
* 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
02In 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
02Provide 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.02 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.
02Ensure company’s medical compliance.
* Act as the sole reviewer to ensure educational grants within02 medical
compliance
* Review and approve promotional materials and activities to ensure their
scientific standard and medical compliance with external and internal
requirements
Qualifications
Must-Have
* Technical
* Therapeutic area knowledge: familiar with the disease knowledge and
clinical practice of the therapeutic area
* Language: Fluent in English02 (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
Nice-to-Have
* Minimum 3+years of experience of clinical practice in Tier 3 hospitals is
preferred
* Preferred experience as Medical Advisor or MSL 02in other multinational
pharmaceutical companies.
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Pfizer is an equal opportunity employer and complies with all applicable equal
employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE

辉瑞公司（Pfizer Inc.）创建于1849年，迄今已有约170年的历史，总部位于美国纽约，是目前全球最大的以研发为基础的生物制药公司。
辉瑞致力于运用创新的科学技术以及全球资源来改善每个生命阶段的健康和福祉，并始终把“携手共创健康中国”作为在华的使命。在中国，我们拥有11,000多名员工， 分布于市场、销售、生产、研发等各个领域；在华累计投资超过15亿美元，拥有两所研发中心与四所工厂；业务遍及全国300多个城市。为了让中国广大患者能及时接受与全球同步的先进的药物治疗，辉瑞未来将进一步加大和加快在华新药引进和上市的力度和速度。
辉瑞生物制药集团（PBG）包含辉瑞旗下所有在专利期以内的创新药品，如抗感染、肿瘤、疫苗、炎症及免疫、抗凝、罕见病等产品线，致力于帮助人们享有更长久、更健康和更美好的生活。
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