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職位描述
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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
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
Qualifications
Must-Have
● 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
Nice-to-Have
● 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.
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
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
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
Qualifications
Must-Have
● 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
Nice-to-Have
● 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.
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
注：聯系我時，請說是在蘿崗人才網上看到的。
工作地點
地址：上海靜安區南京西路中信泰富廣場
求職提示：用人單位發布虛假招聘信息，或以任何名義向求職者收取財物（如體檢費、置裝費、押金、服裝費、培訓費、身份證、畢業證等），均涉嫌違法，請求職者務必提高警惕。
職位發布者
輝瑞HR..HR
輝瑞制藥有限公司
-
制藥·生物工程
-
1000人以上
-
外商獨資·外企辦事處
-
碑林區和平路116號金鼎大廈303
