辉瑞制药-【医学部】 MA Expert-Hematology-北京/上海
Pfizer
辉瑞制药-【医学部】 MA Expert-Hematology-北京/上海
Job Description
MAIN REPONSIBILITIES / DUTIESTo 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 developmentEvaluate hematology products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support new product introduction and line extensionAlign with cross function team including marketing, CCO team, global team etc, develop post marketing research strategy based on Registration/Market needsDevelop medical strategy and implement it to support product developmentDevelop publication plan and implement it As a key partner to provide medical input on business decision makingCo-develop product strategy, positioning, key message with Marketing teamProvide medical support (topic design, KOL communication etc.) on key marketing activitiesProvide 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 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 themSupport on China treatment guideline development, scientific interpretation and promotionPublish or facilitate publication of medical paper in professional journalsCooperation 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 strategyReview and approve all external communication documents to make sure all delivered message are medically precise and consistentCommunicate 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 queryIf 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 complianceReview and approve promotional materials and activities to ensure their scientific standard and medical compliance with external and internal requirementsREQUIRED SKILL SET TechnicalTherapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic areaLanguage: Fluent in English (both spoken and written)Primary Clinical trial knowledgeComputer: Familiar with Microsoft Office softwaresAbility to rapidly catch up global leading edge medical advancementStrong business acumenStrategic thinking and analytic skillsGood interpersonal communication skillsProactive planning and result orientedCustomer focusExcellent Teamwork/CollaborationManagerialSustain Focus on PerformanceAccountabilityManage ChangeAlign Across PfizerEducationClinical Medicine Background in the defined therapeutic area, master degree, Master above is preferredExperience3 years clinical practice in Tier 3 hospitals (corresponding specialty is preferred) or medical affairs experience 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.To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.
Medical
Locations
- China - Beijing - Beijing
- China - Shanghai - Shanghai
Required Qualifications
- Technical (experience)
Responsibilities
- 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 hematology 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
- Develop medical strategy and implement it to support product development
- Develop publication plan and implement it
- Evaluate hematology 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
- Develop medical strategy and implement it to support product development
- Develop publication plan and implement it
- 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
- 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
- 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
- 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
- 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.
- 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).
- 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
- 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
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