Role Description
The MAS role family comprises a variety of medical scientific specialties, such as BU Medical and field based Medical. Be the Pfizer Japan medical scientific point of contact for HCPs, medical societies, regulators, academia and other external stakeholders. Maintain the highest scientific standards, independence and compliance in every medical/scientific external activity, as well as in scope internal processes.
Main Responsibilities
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Demonstrate medical and scientific leadership and expertise.
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Provide and exchange medical/scientific information for/from medical institutions and other related sources in the assigned area and from stakeholders.
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Drive for heightened understanding of the clinical and medical attributes of our products to enhance safe and efficacious use.
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Maintain the highest scientific standards during in/external activities to provide deep medical and scientific expertise.
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Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines/vaccines to address unmet medical needs and fill data gaps.
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Make important contributions to decisions of medical strategies for assigned products to ensure safe, proper, and effective use.
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Contribute to achieving the department/team goals and/or participate in cross-organizational projects as a core member.
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Play an active role in supporting members in the team/organization with the line manager to move towards its goals.
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Develop and execute the medical plan aligned with the medical strategy to meet unmet medical needs in the assigned product(s) and therapeutic area(s).
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Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s) through medical activities such as advisory board meetings and scientific exchanges.
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Create an activity plan as Medical with senior Medical management to address the needs and fill data gaps.
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Develop a Customer Facing Medical Plan in the therapeutic area(s) and asset(s) to establish collaborative scientific relationships with stakeholders.
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Execute the Customer Facing Medical Plan in the assigned area(s)/asset(s) such as unbiased medical and scientific communication with HCPs, medical advisory board meetings, educational seminars, and data generation initiatives.
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Provide subject matter expertise and high-quality scientific exchange, bringing insights into the organization to help shape strategy.
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Collaborate with medical stakeholders as a scientific expert for HCPs, medical societies, academia, and other relevant organizations.
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Establish a strong collaborative scientific relationship through non-promotional activities such as scientific exchanges with relevant stakeholders in the assigned area.
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Develop and maintain a comprehensive stakeholder map to identify relevant HCPs, medical societies, and other relevant external stakeholders.
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Handle UMR (Unsolicited Medical Request) responses, providing accurate, high-quality, and unbiased information to relevant external experts and HCPs.
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Follow up clinical investigator-sponsored research and medical grants compliant with Pfizer policies.
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Acquire extensive medical/pharmaceutical information and gather the latest medical information in the assigned area as a scientific matter expert.
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Deliver key medical and scientific activities within the medical plan, e.g., high-quality educational materials, generation of real-world evidence, non-interventional studies, database studies, and registries.
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Establish a highly reliable, long-term relationship with stakeholders.
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Establish deep and enduring peer-to-peer scientific relationships with leading HCPs and specialists, including non-traditional partners and key decision makers.
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Maintain and enhance the cross-BU alignment on metrics.
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Ensure to collect necessary information and analyze insights prior to the meetings to provide deep medical and scientific expertise to stakeholders and HCPs.
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Provide feedback on information and views obtained from stakeholders and HCPs for related relevant departments in the company.
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Enhance opportunities for creation of evidence based on medical needs by sharing issues in the medical field with internal/external stakeholders.
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Optimize patient centricity of medical communications and deliverables, incorporating Health Literacy and cultural awareness principles.
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Align, contribute, and collaborate with relevant internal stakeholders.
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Provide information on expert/HCP/relevant others feedback on product life cycle strategies to related divisions/departments in the company.
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Collect and analyze unmet medical needs and seek solutions in collaboration with cross-functional colleagues in the company.
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Provide scientific input for scientific meetings and materials.
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Provide medical education programs with and to relevant stakeholders.
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Observe the code of conduct, company’s regulations, and compliance, appropriate communication with related departments, and exercise leadership in POJ.
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Conduct activities in compliance with the MHLW Guidelines for Prescription Drug Sales Information Activities.
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Ensure activities and communications are conducted in compliance with all policies, guidelines, and regulations.
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Ensure awareness of responsibility for reporting adverse events.
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For all Pfizer products, observe applicable laws/regulations and the Pfizer policy, and “Gather and report safety information.”
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Attend training programs on the obligation of assigned safety reporting as appropriate.
Qualifications
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Minimum requirement: 4 year university undergraduate degree and master’s degree in life science, or Pharmacists with a master’s degree or above, or equivalent life science research experience.
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6-year university graduates with pharmacist license, or Nurses with master’s degree or above, or Veterinarians, or Dentists, or MDs.
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Preferred: MD (clinical experience, board certification preferred), or PhD in Life Science.
Requirements
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Medical/pharmaceutical expert knowledge of therapeutic disease area/products.
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Ability to communicate appropriately and build good relationships with internal/external stakeholders.
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Work effectively with teams and across functions by demonstrating Pfizer’s Values & Behaviors.
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Capable of medical discussion with relevant departments and external HCPs.
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Understanding of compliance and relevant laws/regulations in the pharmaceutical industry.
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Able to quickly acquire necessary medical/scientific knowledge and skills through self-learning.
Experience
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Work experience at functions of: Medical Affairs; Development and/or Research preferred.
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Scientific publication experience preferred.
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Medical science liaison experience preferred.
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Clinical research experience.
Language
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Able to understand written and spoken English and Japanese in assigned therapeutic disease area and scientific interactions.
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Minimum TOEIC score of 730 preferred.
Work Location Assignment
リモート – フィールドベース