辉瑞制药-Medical Advisor-抗感染-上海

Pfizer Inc.

Shanghai, China

Job posting number: #7250296 (Ref:pf-4911273)

Posted: May 31, 2024

Job Description

  • Medical Advisor –is the medical professional representing Pfizer in communicating with KOLs and academia for the defined therapeutic areas

    Medical Advisor – is required to support business decision-making in China by providing medical and technical inputs for the defined therapeutic areas

    Medical Advisor – is pro-actively involved in all aspects of a product’s life cycle, from pre-launch to subsequent promotion, through marketing and sales, by providing medical input to enhance the product’s value in all areas of business.

    As such, good understanding and comprehensive knowledge of the defined therapeutic area, proactive attitude and professional behavior are mandatory.

    REQUIRED SKILL SET

    • Technical

    1. Medical Input to Business Decision-Making

    Provide medical inputs in new product planning and product strategic planning

    Sustain Medical expertise for the defined therapeutic areas, by self-studying and internal/external academic training

    Provide timely medical input in product crisis management

    2. Medical Input in product commercial Activity (Marketing, HCBT, Sales)

    Provide medical input to product team in product positioning and differentiation

    Develop publication plan and clinical research proposal for the defined therapeutic areas

    Review and approval promotional materials and promotional activities

    Provide medical inputs in developing training program on disease knowledge in the defined therapeutic areas to sales training group

    Participating National Sales Conferences (POAs) and helping resolve medical issues on products and therapeutic areas

    3. KOL Management

    Set up and update KOL database for the defined therapeutic areas

    Regular communication with KOLs to share most updated medical information in the defined therapeutic areas

    Facilitate KOL in publishing articles in top national or international academic journals and national conference in the defined therapeutic areas

    4. Cooperation with local medical association

    Provide necessary input from product and therapeutic perspective, to assist collaboration programs with local Medical associations and other academic or government agencies

    Assist to review and approval of Investigator Initiated Research applications.

    5. Lecture delivery and product training

    Regular lecture, to share most updated clinical trial data, interpreter treatment guideline and provide summary of product efficacy and safety profile.

    Product training to internal and external customers, including LT, sales and KOLs.

    6. Medical Information

    Provide medical input to medical information team in setting up medical query responding systems Liaise between business team and medical information team, to ensure timely delivery of medical information Provide timely responses to both internal and external customers’ queries on the information of Pfizer’ s in-market and pre-launched products and relating therapeutic areas Provide medical input to Safety Officer in handling Pfizer’s product safety information Proactively provide the latest medical information to internal and external customers on regular basis.

    7. Medical Input in Drug Registration Activities

    Timely review and approve local product labeling for all Pfizer products Provide medical input in feasibility studies for global trials Review and approval of phase IV clinical trial application based on Market needs Officially input on study site selection from commercial prospective Join protocol synopsis and study report discussion/finalization meeting, to get the first hand information about local new product clinical development

    8. Safety responsibilities

    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 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.

    • Education
    • Medical Background, clinical practice experience in the defined therapeutic area is preferred
    • Experience
    • 1 year medical affairs experience in other multinational pharmaceutical companies is preferred Good medical knowledge for the defined therapeutic area Good understanding about pharmaceutical business Proficiency in English and good computer usage

 
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

#LI-PFE


Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.


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More Info

Job posting number:#7250296 (Ref:pf-4911273)
Application Deadline:Open Until Filled
Employer Location:Pfizer Inc.
New York,New York
United States
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