【医学部】（Sr.）MA-代谢领域-北京或上海

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.