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Insmed

Develops therapies for rare diseases

Medical Strategy Lead - NTM

Biology & BiotechPosted on Nov 13
Full-timeJapanNo salary listed

About the Job

Requirements

  • A minimum of 10–15 years of successful Medical/Scientific Affairs experience at a pharmaceutical or biotechnology company in Japan in a global setting.
  • Solid experience managing cross-functional teams of senior medical/scientific experts and operational/administrative professionals.
  • Fluency in Japanese at a native level and high-level business fluency in English.
  • Adherence to high ethical standards and a solid understanding of applicable local and global policies, rules, regulations, and pharmaceutical-industry compliance requirements in Japan.
  • Strong understanding of pharmaceutical business, including drug research and development, manufacturing, and commercialization.
  • Strategic and logical thinking, effective analytical skills, strong organization, and attention to detail, clarity, accuracy, and conciseness.
  • Ability to understand and discuss subjects at the intersection of medicine and policy, connect science, medicine, and unmet medical needs to Medical Affairs strategy, and communicate complex scientific information and data effectively in Japanese and English.
  • Ability to present ideas and influence and negotiate with others to achieve goals.
  • Ability to work productively across local and global organizations and influence without authority.
  • Ability to demonstrate the company’s core values, mission, vision, value proposition, and position-specific competencies.

Responsibilities

  • Partner with Medical Affairs leadership, Medical Affairs teams, local and global internal business partners, commercial partners, and external stakeholders to plan and execute the brand plan and strategies and tactics defined in the Japan Medical Affairs Plan for the product.
  • Develop and provide valuable information and insights to internal and external stakeholders through in-depth, up-to-date understanding of the product, its indications, therapeutic area, and technologies, ensuring high-quality science in Medical Affairs duties.
  • Lead, manage, and coordinate development and implementation of the Japan Medical Affairs Plan with Japan Medical Affairs teams and internal and external stakeholders, ensuring activities are delivered on scope, on time, and on budget in compliance with applicable laws, regulations, policies, procedures, and requirements.
  • Lead, manage, coordinate, and facilitate engagement among internal and external stakeholders, including scientific leaders, healthcare professionals, congresses, and medical, academic, and professional societies; ensure compliant, professional, and balanced exchange of scientific, medical, and business information and insights; and translate those insights into strategy and tactics.
  • Conduct competitive intelligence to provide inputs and insights for planning, executing, and updating the Japan Medical Affairs Plan.
  • Lead local medical and commercial review and decision processes, including Japan medical, commercial, and grant review committees and review of medical information letters, and contribute to global review processes and meetings.
  • Partner with clinical development functions on clinical-development strategy and planning, including engagement with the Pharmaceuticals and Medical Devices Agency and Ministry of Health, Labour and Welfare, and medical review of clinical and regulatory documents such as Japanese INDs, NDAs, and PSURs.
  • Support identification and selection of external medical experts, assessment of clinical sites and investigators, and patient recruitment for clinical studies in collaboration with Clinical Trial Operations.
  • When licensed to practice medicine in Japan, act as an in-house medical expert, providing medical guidance and expert opinion, including for drug safety, pharmacovigilance, and product-quality surveillance.
  • Partner with internal functions and external stakeholders to lead and support local business in Japan.
  • When assigned, manage Japan Medical Affairs staff and teams.

Desired Qualifications

  • Experience with Japanese IND and NDA processes, NHI pricing negotiation, product launch excellence, and pharmaceutical product lifecycle management in Japan.
  • Knowledge and experience in pulmonary, infectious, and/or cardiovascular diseases.
  • Experience in rare and/or neglected diseases.

About the Company

Insmed

Develops therapies for rare diseases

Insmed focuses on developing and delivering therapies for serious and rare diseases. Its products come from a pipeline of clinical trials and approved treatments, sold to patients in global markets with offices in Bridgewater, NJ, Europe, and Japan. The company’s work combines research and development, regulatory approvals, and commercialization to bring therapies from discovery to patients. Insmed differentiates itself by addressing unmet medical needs in rare diseases and maintaining a global infrastructure that supports development, approval, and patient access. The goal is to improve patient outcomes by providing effective treatments for conditions with limited existing options.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Bridgewater Township, New Jersey
Founded
1988

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