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【AstraZeneca】【Medical】Associate Medical Affairs Lead, ﾒﾃﾞｨｶﾙ本部 オンコロジー部門 LC/IO領域

AstraZeneca · Minato-ku, Tokyo, Japan · Global

Medical Affairs
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Not yet analysed
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Demand80
Career growth85
Healthcare fit85
Remote potential30
5-year outlook
Competitive for pharma Medical Affairs in Japan; likely includes base plus bonus and benefits, with growth into Medical Affairs Lead or Director roles. Exact figures vary by experience and company, but this is a senior-track position.
Clinical license
Not required
Applicant reach
narrow
Seniority
mid
Employment type
full-time
Date found
2026-09-06

Intelligence details

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Why this is worth applying to

Strong opportunity for clinicians with oncology research experience seeking a non-clinical pharma career. The role leverages clinical expertise in a strategic, high-impact setting, but requires Japanese fluency and a long-term commitment to the industry.

Who should apply

Oncologists, hematologists, or pharmacists with 3+ years of clinical or research experience in oncology, especially those with publication or investigator-sponsored study involvement. Also suitable for PhDs in life sciences with strong clinical knowledge.

CV angle

Highlight oncology clinical/research experience, publication track record, study design and protocol review, regulatory knowledge, and cross-functional collaboration. Emphasize ability to communicate with Key External Experts and manage complex projects.

Skills to highlight

  • Clinical research design
  • Publication writing and management
  • Investigator-sponsored study oversight
  • Regulatory compliance (ICH-GCP, local laws)
  • Stakeholder engagement
  • Project management
  • Data analysis and interpretation
  • Cross-cultural communication (Japanese/English)

Role summary

Associate Medical Affairs Lead at AstraZeneca's oncology division, responsible for driving evidence generation activities (company- and investigator-sponsored studies), publication planning, and educational program execution in the LC/IO (lung cancer/immuno-oncology) area. Collaborates with internal and external stakeholders to ensure compliant, high-quality scientific output.

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