Jobs for People with MS: National MS Society

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Amgen Country Medical Affairs Lead (CMAL) Bone–Associate Director in Tokyo, Japan

To maximize Amgen's value propositions through first class medical and scientific expertise with key scientific customers as a representative of (product name) MA team

To develop and implement Brand/medical affairs plan with cross functional collaboration by managing (product name) MA team

As a Single Point of Contact for (product name) MA team, CMAL is responsible for

  1. Strategic Leadership:
  • Development and execution of brand/medical affairs plan and activity tracking in Therapeutic Area(TA) that includes but not limited to:

  • Evidence generation plan

  • Scientific engagement plan (SEP)

  • Scientific event plan

  • Active contribution to product/TA strategy and internal projects

  1. Medical Initiatives:
  • Lead and oversee the planning, development, and execution of medical initiatives and projects within the therapeutic area.

  • Ensure the effective implementation of medical programs to support the company's goals.

  1. Scientific Expertise:
  • Serve as a subject matter expert in the therapeutic area, staying abreast of scientific and clinical developments, and providing insights to internal stakeholders.

  • Collaborate with cross-functional teams to integrate scientific knowledge into medical affairs programs.

  1. Team Leadership:
  • Lead and manage a team of medical professionals, providing guidance, mentorship, and support.

  • Foster a culture of excellence, collaboration, and continuous learning within the medical affairs team.

  1. Collaboration and Networking:
  • Foster collaborative relationships with external key opinion leaders, healthcare professionals, and other stakeholders in the therapeutic area.

  • Collaborate with internal teams, including clinical development, regulatory affairs, and marketing, to achieve common goals.

  1. Pipeline:
  • Active contribution to TA pipeline and product LCM
  1. Compliance and Ethics:
  • Ensure that all medical affairs activities adhere to regulatory compliance, ethical standards, and company policies.

  • Provide guidance on compliance issues to the team.

Requirements:

  • Advanced degree (e.g. PhD, MD) preferred or strong demonstration of equivalent combination of relevant educational and professional training

  • Medical or scientific education or experience from similar positions

  • Minimum 5 years of experience in industry or research institute in relevant TA etc.

  • Minimum 5 years of experience in Medical affairs or R&D

  • Experienced in team/people management

  • Excellent verbal and written communication skills including the ability to clearly and effectively present information

  • Proficient in written and spoken English

  • Proven scientific expertise in relevant TA, related products, disease state, and educated on latest discoveries

  • Knows medical affairs business processes

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