Medical Advisor

3 weeks ago

Beijing, Beijing, China Pfizer Full time

Job Summary

We are seeking a highly skilled Medical Advisor (Senior) to join our team at Pfizer. As a key member of our organization, you will play a critical role in developing and implementing medical strategies to support our business objectives in the urological tumor field.

Responsibilities

  • Develop and execute medical development and life-cycle management strategies for inline products and pipeline within Pfizer China business objectives and strategy.
  • Provide state-of-the-art medical expertise to assist business decision-making, establishing platforms and channels with China academic organizations in defined therapeutic areas to deliver Pfizer products' messages to key influencers and stakeholders.
  • Build effective medical advisor interfaces and provide professional medical training to support commercial teams in achieving their objectives, ensuring the scientific validity and medical compliance of company activities.
  • Evaluate new products, new indications, new research programs, and new business potentials of defined therapeutic areas from a medical perspective to support new product introduction and line extension.
  • Align with cross-functional teams, including marketing, CCO teams, and global teams, to develop post-marketing research strategies based on registration/market needs.
  • Provide phase IV study direction and develop key elements, design and manage local non-interventional studies (NIS) as a clinician, and develop medical strategies to support product development.
  • Develop publication plans and implement them, evaluate and review investigator-initiated research proposals to ensure their scientific standards and strategy fit.
  • Co-develop product strategies, positioning, and key messages with marketing teams, provide medical support on key marketing activities, and provide broad and deep medical insights/summary documents of defined therapeutic areas to business partners.
  • Review and approve local standard response letters to healthcare professionals, develop sales force medical capabilities through training program design, lecture delivery, and periodic medical knowledge updates in different settings through various channels.
  • Support drug registration activities, including timely review and approval of local product labeling (LPD), developing medical justification documents to support LPD-related queries from governments, and providing medical input in feasibility evaluations of studies for global trials.
  • Establish cooperation and partnerships with medical associations to promote medical advancements, set up national-level KOL databases, and maintain medical communication with key opinion leaders through various approaches.
  • Design educational programs for top KOLs and implement them, support China treatment guideline development, scientific interpretation, and promotion, publish or facilitate publication of medical papers in professional journals, and cooperate with local medical societies to conduct medical programs/conferences to introduce new concepts and state-of-the-art medical progress to China.
  • Maintain company image and protect patient welfare by working with cross-functional teams on crisis management, performing medical evaluations, explanations, and developing medical justification or responding documents.
  • Provide medical expert opinions on company responding strategies, review and approve all external communication documents to ensure medically precise and consistent messages, and communicate with external customers directly for medical issues as necessary.
  • Provide medical expert opinions in safety events management to avoid negative impacts, provide professional medical consultations to safety officers to solve Pfizer products' safety queries, and perform clinical safety oversight, including regular reviews of individual subject safety data and cumulative safety data with safety risk leads.
  • Ensure company medical compliance by acting as sole reviewers for educational grants within medical compliance, reviewing and approving promotional materials and activities to ensure scientific standards and medical compliance with external and internal requirements.

Qualifications

  • Technical
  • Therapeutic area knowledge: familiar with disease knowledge and clinical practice of the therapeutic area
  • Language: fluent in English (both spoken and written) is preferred
  • Primary clinical trial knowledge
  • Computer: familiar with Microsoft Office software is preferred
  • Ability to rapidly catch up with global leading-edge medical advancements
  • Strong business acumen
  • Strategic thinking and analytic skills
  • Good interpersonal communication skills
  • Proactive planning and result-oriented
  • Customer focus
  • Excellent teamwork/collaboration
  • Managerial
  • Sustain focus on performance
  • Accountability
  • Manage change
  • Align across Pfizer
  • Education
  • Clinical medicine background in the defined therapeutic area, master's degree or above is required

Preferred Qualifications

  • Minimum 3+ years of experience in clinical practice in Tier 3 hospitals is preferred
  • Preferred experience as Medical Advisor or MSL in other multinational pharmaceutical companies

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