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Pfizer Regional Medical Advisor (MSL)_Vaccines in Beijing, China


Maximize the value of Pfizer products to Chinese patients and health care professional through medical activities in regional level. Implement medical/research/disease management programs; introduce new concept through medical education to help doctors to improve patients' outcome; conduct medical to medical communication to transport product knowledge and therapeutic update to key influencers and stakeholders; and provide professional medical training to commercial teams.

1. Implementation medical programs and activities in fields

  • Support Pfizer sponsored Non interventional study and other medical programs at regional level.

  • Design and conduct disease management program according to timeline and with good quality.

  • Discuss research concept with interested researcher, and communicated the nature and requirement of Pfizer's Investigator Sponsored Research (ISR)/Clinical Research Collaborations (CRC) based on ISR/CRC strategies

  • Facilitate submission of investigator initiated pre-clinical and clinical proposals, and act as a liaison between Pfizer and ISR/CRC researcher; and follow up ISR/CRC on its progress according to timeline

2. Lead medical to medical communication in the fields

  • Lead and develop regional level medical strategy in the designated therapeutic area

  • Set up KOL database in responsible region and conduct regular medical communication.

  • Organize regional level medical to medical meetings and activities with KOLs to deliver cutting edge medical information of designated therapeutic area and assigned products

  • Conduct medical educational meeting to introduce new concept to help doctors to improve patients' outcome and advance their research capability

  • Present at medical communication meeting at national and regional level.

  • Provide timely feedback of KOL's comments and insights to supervisors and relevant Medical Advisors

  • Respond medical inquiries as needed.

  • Establish good academic relationship with regional academic origination at designated therapeutic area.

  • Cooperate and align with Medical Advisors to engage KOLs

3. Improve sale team medical ability through medical training ,lecture delivery and medical knowledge

  • Orgnize face to face meeting or Webex meeting to cadcade medical information to improve sales team's medical knowledge.

  • Provide customized response for common medical queries in the field for assigned products.

  • Present at POA and regional sales meetings for medical information

4. Medical input to product medical and brand plan

  • Collect, analyze and report timely local customer medical insights to input on product strategy and message development

  • Work with (Senior) Medical Advisor and product manager proactively to assist product strategy implementation

5. 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 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 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

6. Ensure company's medical compliance

  • Implement medical programs and activities within medical compliance

  • Communicate medical information with compliance

  • Ensure timely SOP learning, and daily practice compliant with SOPs.


  • 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

  • Computer: Good at Microsoft Office software

  • Strong business acumen

  • 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

  • Develop People

  • Align Across Pfizer

  • Certifications

  • N/A

  • Education

  • Public health, medical or pharmaceutical Background, master degree or above. M.P.H. or M.D. in the defined therapeutic area is preferred

  • Experience

  • About 3 years clinical practice or medical affairs experience in other multinational pharmaceutical companies is preferred.

  • Good medical knowledge in the defined therapeutic area.

  • Good understanding about pharmaceutical business, medical affairs experience or clinical studies experience in multinational pharmaceutical companies

  • Proficiency in English and good computer skills

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