The main responsibilities include: Maximize the value of Pfizer inline vaccines to Chinese people within Pfizer’s vision and mission; Develop China (including Hong Kong and Macau) medical development and life-cycle management strategy for inline and pipeline within China business objectives and strategy; Provide medical and clinical expertise to drive Pfizer clinical trials; Conduct epidemiology studies and real world studies; Establish platform and channel with China academic organization and health care workers in public health to conduct academic communication to key influencers and stakeholders. Build effective medical advisor interface and provide professional medical training to support commercial teams to achieve their objectives.
- Lead and develop product life-cycle management strategy from medical perspective to maximize products value and long term development
l Develop effective medical plan for the public area and defined therapeutic area(s) aligning with products development strategy and ensure its timely execution
l Identify medical opportunity in current trends of diagnosis, existing/emerging treatment options , and unmet medical needs in public health and defined therapeutic area(s) as medical base for business initiative and decisions
l Evaluate new products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support business decisions
l Develop epidemiology study plan to support the defined therapeutic area(s)
l For defined therapeutic area(s), develop post marketing research strategy, evaluate and endorse phase IV study direction, local Non-interventional Study (NIS) study, and Investigator Initiate researches, based on registration/market needs in alignment with cross function team including marketing, and global team
l For defined therapeutic area(s), develop and execute publication plan, provide input to the publication plan, provide ideas for generating manuscripts of scientific interest, and actively review manuscripts and abstracts to ensure medical and scientific accuracy
l Work with commercial teams on therapeutic strategies and key issues resolution from medical point of view
l Review and approve medical dossier, briefing documents for internal review or external submission
l Provide medical input to MI team
l Update to internal and external customer and answer complicated medical queries
l Cooperate with global/ICD team to obtain resources for the development of product lines
- Support products registration activities
l Define the unmet medical needs, data gap and strategy to meet the gap
l Provide medical advice to registration trials protocol synopsis and study report
l Review and approve of local product labeling (LPD)
l Review and approve medical justification document to support LPD related queries from drug administration agency
l Provide medical input in feasibility evaluation of global and local trials
l Provide official input on study site selection from therapeutic perspective
- Enhance the delivery of new concept and Pfizer products key message to key influencers /stakeholders, and establish cooperation and partnership with medical association to promote medical advancement
l Set up top national level KOL database, and effective medical communication plan through various approaches , and ensure its implementation
l Establish strategic partnership with medical association/institute through appropriate medical programs
l Cooperate with local medical association to facilitate new concept and the state of the art medical progress
l Provide medical support to China clinical practice guideline development, scientific interpretation and promotion
- Act as a core member to work with cross function team on crisis management to maintain company’s image and protect patient’s welfare
l Approve medical responding document
l Provide medical expert opinion and guidance on company responding strategy
l Review and approve external communication documents to make sure all delivered message are medically precise and consistent
l Communicate with external customers directly for medical issues as necessary
- Ensure company’s medical compliance
l Act as the 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
Requirements
· Technical
o Therapeutic area knowledge: familiar with the public health knowledge and clinical practice of the therapeutic area
o Language: Proficiency in oral and written English
o Good understanding about pharmaceutical business
o In-depth epidemiology study, RWE, Clinical trial knowledge
o Computer: Good at Microsoft Office software
o Cross functional leadership skill
o Strong communication and influencing skill
· Education
Master degree or above, major in public health or preventive medicine or clinical medicine
· Experience
o Experience in preventive medicine areas (CDC/vaccine, surveillance, epi study, RWE study is preferred)
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical