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Pfizer

Makes cancer drugs, vaccines and other medicines

Office-based Medical Affairs Scientist - Multiple Teams

Biology & BiotechConfirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listedIn-person

About the Job

Requirements

  • A four-year university undergraduate degree and a master's degree in life science, or a qualifying professional education route: a pharmacist with a four-year university degree, pharmacist license, and master's degree or equivalent life science research experience; a pharmacist with a six-year university degree and pharmacist license; a nurse with a master's degree; a veterinarian; a dentist; or an MD.
  • Medical and pharmaceutical expert knowledge of the therapeutic disease area and products.
  • Ability to communicate appropriately and build good relationships with internal and external stakeholders.
  • Ability to collaborate effectively across teams and functions, demonstrating the company’s values and behaviors and agility to learn from others.
  • Ability to conduct medical discussions with relevant departments and external healthcare professionals.
  • Understanding of compliance and relevant pharmaceutical-industry laws and regulations, and ability to advocate appropriate product use.
  • Knowledge and understanding of internal organizational structure, key stakeholders, and strategies.
  • Ability to acquire necessary medical and scientific knowledge and skills through self-learning.
  • Ability to understand written and spoken English and Japanese in the assigned therapeutic disease area and scientific interactions.
  • Minimum TOEIC score of 730.

Responsibilities

  • Serve as Pfizer Japan’s medical scientific point of contact for healthcare professionals, medical societies, regulators, academia, and other external stakeholders.
  • Identify unmet medical needs, contribute to building and executing medical plans, and establish clinical evidence as a scientific and medical leader.
  • Maintain high scientific standards during internal and external activities and provide deep medical and scientific expertise.
  • Develop local medical plans aligned with global medical plans to address local unmet medical needs and data gaps, and contribute to local medical strategies and lifecycle clinical plans for inline and pipeline medicines and vaccines.
  • Provide and exchange medical and scientific information with medical facilities in the assigned area and external stakeholders; contribute to medical strategy decisions for assigned products to support safe, proper, and effective use.
  • Increase understanding of disease burden in the assigned therapeutic area and the medical attributes of products to enhance safe and efficacious use.
  • Contribute to department and team goals, participate as a core member in cross-organizational projects, and provide guidance to deliver results.
  • Identify unmet medical needs and healthcare disparities for assigned assets and therapeutic areas, and execute customer-facing medical activities, including unbiased scientific communication, advisory board meetings, educational seminars, data-generation initiatives, and medical-material creation with necessary scientific input.
  • Create activity plans with senior medical management to address unmet needs and data gaps.
  • Develop the customer-facing component of medical plans for assigned therapeutic areas and assets to establish collaborative scientific relationships with stakeholders.
  • Provide subject-matter expertise and high-quality scientific exchange, and bring formal and informal insights into the organization to shape strategy.
  • Establish collaborative scientific relationships through non-promotional scientific exchanges with relevant stakeholders, including discussions of current research papers and follow-up on academic conference presentations.
  • Maintain a comprehensive stakeholder map of relevant healthcare professionals, medical societies, and other external stakeholders, and communicate with them effectively at an expert level.
  • Follow up on clinical investigator-sponsored research and medical grants in compliance with company policies.
  • Acquire and maintain current medical and pharmaceutical information in assigned areas to identify unmet needs and support medical strategy.
  • Deliver medical-plan activities, including educational materials, real-world evidence, non-interventional studies, database studies, and registries in collaboration with the Health & Value team, and ensure timely publication of data.
  • Share customer insights with internal and external stakeholders through cross-functional partnership to enhance opportunities for evidence generation based on medical needs.
  • Apply health-literacy and cultural-awareness principles to medical communications and deliverables to keep patients central.
  • Establish peer-to-peer scientific relationships with leading healthcare professionals and specialists, including non-traditional partners and key decision makers.
  • Maintain and enhance cross-business-unit alignment on metrics.
  • Collect necessary information and analyze insights before meetings to provide medical and scientific expertise to stakeholders and healthcare professionals.
  • Provide expert and healthcare-professional feedback on product lifecycle strategies to relevant company divisions and departments.
  • Share medical and scientific information and insights appropriately with Marketing colleagues to support brand-plan development.
  • Provide scientific input for scientific meetings and materials.
  • Provide medical education programs with medical societies or relevant stakeholders.
  • Provide medical and scientific input into protocol-feasibility assessments for clinical-trial proposals.
  • Collaborate with Development Japan and global development to identify appropriate investigators and sites for company-sponsored clinical trials.
  • Work with clinical research and Development Japan colleagues, and above-country and global business-unit colleagues, to support timely completion of company-sponsored clinical trials.
  • Provide scientific and medical leadership and input to global clinical teams and Development Japan to ensure trial design and selection reflect Japan’s needs, using customer and patient insights; support clinical development programs and regulatory interactions from early development.
  • Contribute to development and implementation of product and therapeutic-area medical strategies, and provide medical and scientific advice internally and externally to support appropriate product use and patient safety in alignment with business goals.
  • Provide accurate, high-quality, unbiased medical information to healthcare professionals and external experts, including managing unsolicited medical requests.
  • Provide scientific insight and support to field- and head-office-based commercial colleagues.
  • Collaborate with cross-functional in-country and above-country teams to develop impactful, compliant promotional and non-promotional materials for customers.
  • Collect and share insights from healthcare professionals and stakeholders to inform medical strategy and business opportunities.
  • Manage local advisory boards to gain customer insights.
  • If media-trained, present the scientific perspective on selected topics during media briefings.
  • Follow the Medical Affairs code of conduct for external medical interactions, provide promotional or non-promotional explanations as appropriate, and comply with the Ministry of Health, Labour and Welfare guidelines for prescription drug sales information activities.
  • Ensure activities and communications comply with all policies, guidelines, and regulations.
  • Observe applicable laws, regulations, and company policy for all products, gather and report safety information, and attend safety-reporting training as appropriate.
  • As needed, collaborate with Japan Medical Lead, Japan Medical Product Lead, global Medical Affairs members, and relevant functions to identify unmet medical needs and candidate therapies for potential interventions in Japan through medical activities such as advisory boards and consultations with medical experts, while maintaining confidentiality.
  • As needed, respond rapidly to critical supply issues from a medical perspective, including rapid communications with academic societies and regulatory authorities.

Desired Qualifications

  • An MD with clinical experience; board certification is preferred.
  • A PhD in life science.
  • Medical Affairs or Development Japan experience and/or research experience.
  • Scientific publication experience.

About the Company

Pfizer

Makes cancer drugs, vaccines and other medicines

Pfizer discovers, makes, and sells prescription medicines and vaccines for patients, doctors, and governments worldwide, with large businesses in vaccines, cancer, heart disease, and rare diseases. In 2020, its COVID-19 shot, developed with German partner BioNTech, became the first COVID-19 vaccine authorized in the United States. Its scientists find drug candidates and run clinical trials to prove they are safe and effective, and Pfizer then manufactures approved products in its own plants, earning most of its money from patented drugs before cheaper generic copies arrive. Pfizer was founded in 1849 as a chemicals business in Brooklyn and is based in New York City.

Company size
10,001+
Company stage
IPO
Headquarters
New York City, New York
Founded
1849

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