• 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 oversightincluding 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

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