Roles summary

Strategic planning and development of external stakeholder strategy, execution of external medical to medical engagement according to business unit medical strategy, and alignment with Country Medical Leads on implementation and delivery of medical projects.

Lead medical to medical communications in the field. This role considered as field base medical activities with at least 50% of time in customer interaction (applied for person with out people management).

The Medical Lead is responsible for ensuring consistency, quality, and compliance in execution of medical to medical initiatives and stakeholder-centric engagement.

The Medical Lead is also responsible for quantifying field medical impact and monitoring or not Medical Science liaison (MSLs) and medical BU performance management to maximise the impact of medical activities.

• External Medical and Scientific engagement strategy and implementation
  • Plans and executes medical scientific strategic plans, as per their specialty assigned role
  • Support development of medical field strategy for external stakeholder engagement related to specified specialty/BU.
  • Medical stakeholders management: establish and strengthen medical and scientific relationship between Medical Lead and external stakeholders e.g. KOLs, medical Societies and medical schools
  • Seeking and developing awareness of external medical community to drive exceptional HCP discussion and insights and shape medical trends toward innovative medicine treatment.
  • Ensure effective data communication and medical insight capturing
  • Execute or Collaborate with Medical Lead on conduct of advisory boards; organization and delivery of relevant educational/training workshops/meetings; and participation in medical/scientific conferences.
• Lead and work together with X-Category Medical Team to develop pre-launch strategy and decide pre-launch road map, develop a medical plan in order to ensure pre-launch excellence
• Collaborate with X-functions (Medical information, Centre of Excellence, and BUs) to develop and apply the relevant medical materials for M2M communication
  • Develop, monitor and report KPIs in relation to field-based medical activity
• External Collaboration Projects:
  • Ensure timely and efficient communication to complete required internal/external process including system administration, maintain good documentation, tracking, payment, material, and drug shipment in a timely manner.
  • Provide medical input to collaboration project lead by other Medical colleagues (e.g. Medical Outcomes and RWE Scientist) or other cross-functional team
• Pfizer-Sponsored Research or Investigator-sponsored research:
  • Ensure compliance of operational requirements
  • Discuss research concept with interested researcher, and communicate the nature and requirement of Pfizer's ISR.
  • Facilitate submission of investigator initiated pre-clinical and clinical proposals, and act as a liaison between Pfizer and ISR researcher.
  • Facilitate research proposal screening and study placement and follow up activities.
  • Collaborate with Medical Outcomes & RWE Scientist to support Pfizer Regional or local sponsored trial (including post-marketing trial), which is not under the clinical research team, if applicable.
• Training and Development
  • Provide disease(s), product(s) or basic pharmacology training to other relevant colleagues, as required
  • To assist commercial and other relevant department to deliver training to external stakeholders upon request
  • Participate in both internal and external training/meetings recommended by supervisor to improve efficiency, competency and/or for future career development.
  • Solicit and consolidate feedback from external and internal stakeholders in relation to team effectiveness, quantify and communicate the value and effectiveness of field-based medical activities
• Other Medical Affairs projects as defined by the Country Medical Director

• Tertiary education in medicine; relevant specialty training desirable
• Industry, clinical, research or academic experience; with track record of publications preferred
• Knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines
• Previous experience in medical affairs, clinical affairs or regulatory affairs in the pharmaceutical industry preferred
• Capability of strategic insight to drive new businessdirection from medical perspective
• Expertise in clinical trial design and methodology, and understanding of interfaces, and conduct preferred
• Working experience in medical project; launch strategy
• Good communication skills, both written and verbal (including medical writing and presentation skills) and proficiency in English
• Analytical skills and reasoning, and sound medical judgment/decision making
• > 5 years' experience in medical affairs role