辉瑞制药-【医学部】 MA Expert-Hematology-北京/上海

MAIN REPONSIBILITIES / DUTIES

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

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

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

REQUIRED SKILL SET

Technical

Therapeutic area knowledge: familiar with the disease knowledge and clinical practice of the therapeutic area

Language: Fluent in English  (both spoken and written)

Primary Clinical trial knowledge

Computer: Familiar with Microsoft Office softwares

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 preferred

Experience

3 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