• 招聘类型：社招
• 工作性质：全职

职位描述

MAIN REPONSIBILITIES / DUTIES

Maximize the value of Pfizer products to Chinese patients and health care professional within Pfizer’s vision and mission. Develop China medical development and life-cycle management strategy for inline products and pipeline within Pfizer China business objectives and strategy. Provide state of the art medical and clinical development expertise to drive Pfizer clinical trials. Establish platform and channel with China academic organization in defined therapeutic area to delivery Pfizer products message to key influencers and stakeholders. Build effective medical advisor interface and provide professional medical training to support commercial teams to achieve their objectives.

1. Lead and develop product life-cycle management strategy from medical perspective to maximize product’s value and long term development.

Develop and execute medical plan for the defined therapeutic area(s) aligning with products development strategy

Identify medical opportunity in current trends of diagnosis, existing/emerging treatment options , and unmet medical needs in defined therapeutic area as medical base for business initiative and decisions

Evaluate new products, new indications, new research programs, new business potentials of defined therapeutic areas from medical perspective to support business decisions

Develop post marketing research strategy based on registration/market needs in alignment with cross function team including marketing, CCO team, and global team

Evaluate and endorse phase IV study direction, and drive its endorsement from company

Oversee and manage local Non-interventional Study (NIS) study

Review and endorse Investigator Initiate research proposal to ensure its scientific standard and strategy fit

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

Work with BU marketing and sale leaders on therapeutic strategies and key issues resolution from medical point of view

Review and approve medical dossier for drug reimbursement listing, pricing bidding and other access related issues.

Coach and guide the team to provide medical input to MI team on LSRD

Coach the team to communicate medical update to internal and external customer and answer complicated medical queries.

2. Develop sale team medical capability through medical training ,lecture delivery and medical knowledge update through various channel

Coach and guide team to design/conduct effective training programs on field force supporting programs to develop sale team’s medical capability, and solve key medical issues.

3. Support products registration activities

Provide medical advice to registration trials protocol synopsis and study report

Review and approve of local product labeling (LPD)

Review and approve medical justification document to support LPD related queries from drug administration agency

Provide medical input in feasibility evaluation of global and local trials

Provide official input on study site selection from therapeutic prospective

4. 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

Guide team to set up top national level KOL database, and effective medical communication plan through various approaches , and ensure its implementation

Establish strategic partnership with local medical association through appropriate medical programs

Cooperate with local medical association to facilitate new concept and the state of the art medical progress

Coach and guide the team to provide medical support to China clinical practice guideline development, scientific interpretation and promotion

5. Act as a core member to work with cross function team on crisis management to maintain company’s image and protect patient’s welfare

Coach and develop team to perform medical evaluation, explanation on the event

Approve medical responding document

Provide medical expert opinion and guidance 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

6. Provide medical expert opinion in safety events management to avoid negative impact

Coach the team to 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 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 SAF 09 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.

7. 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.

任职条件

REQUIRED SKILL SET

• Technical

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

 Language: Proficiency in oral and written English

 Good understanding about pharmaceutical business

 In-depth Clinical trial knowledge

 Computer: Good at Microsoft Office software

 Strong business acumen

 Capability of strategic insight to drive new business direction from medical perspective

 Cross functional leadership skill

 Strong communication and influencing skill

• Managerial

 Sustain Focus on Performance

 Create an Inclusive Environment

 Encourage Open Discussion and Debate

 Manage Change

 Align Across Pfizer

• Certifications

N/A

• Education

  Master degree major in clinical medicine, Medical doctoral degree or PHD in medical is preferred

  Master of Business Administration is a plus

• Experience

 3 years clinical practice in Tier 3 hospitals (corresponding specially is preferred)

 MD or PHD with 3+ years medical affairs experience in multinational pharmaceutical companies experience, or

 Master with 5+ years experience, or Management experience preferred

职位要求

• 学历要求：无
• 工作经验：无
• 外语要求：不需要