【astrazeneca】【r&d】patient Safety Epidemiologist, 研究開発本部 ﾍﾟｲｼｪﾝﾄ ｾ-ﾌﾃｨ統括部 ﾍﾟｲｼｪﾝﾄｾｰﾌﾃｨｴﾋﾟﾃﾞﾐｵﾛｼﾞｰ＆ｴﾋﾞﾃﾞﾝｽｼﾞｪﾈﾚｰｼｮﾝ部

AstraZeneca

Osaka, Japan
Onsite (osaka or tokyo)
Post authorization regulatory commitment studies
Real-world evidence generation
Secondary data analysis
AstraZeneca is seeking a Patient Safety Epidemiologist in Osaka or Tokyo, Japan, to lead post-authorization regulatory commitment studies and generate real-world evidence. The ideal candidate will possess extensive experience in pharmacoepidemiology, strong leadership skills, and a commitment to high ethical standards

Job Summary

  • The PS Epidemiologist (PSEPI) serves as a study lead for Post Authorization Regulatory Commitment Studies (PARCS) including post-marketing database study and use-result survey, accelerating the generation of valuable real-world evidence.
  • As an expert in epidemiological research, the PSEPI leads the education and utilization of real-world data within the Japan Patient Safety organization and contributes to organizational development.
  • In study execution and publicizing study results, the PSEPI leads regulatory processes, including epidemiological consultations, and engages with internal and external stakeholders.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Patient Safety Epidemiologist in Osaka or Tokyo, Japan, to lead post-authorization regulatory commitment studies and generate real-world evidence. The ideal candidate will possess extensive experience in pharmacoepidemiology, strong leadership skills, and a commitment to high ethical standards.

Skills & Requirements

Must-have

  • Post Authorization Regulatory Commitment Studies
  • Real-world evidence generation
  • Secondary data analysis
  • Epidemiological research methodologies
  • Cross-functional leadership
  • Vendor management

Nice-to-have

  • Continuous improvement of deliverable quality
  • External presentations and publication support
  • Cost-effectiveness and budgeting
  • Drug development lifecycle management

Key Requirements

  • 2+ years pharmacoepidemiology experience (PhD) or 5+ years (Masters)
  • Experience authoring/reviewing observational study protocols/CSRs
  • Experience conducting Japanese database studies (claims, DPC, EMR)
  • Experience conducting global meetings in English
  • MPH or MSc in relevant field
  • Business English Level

Work Rights

Not specified

Tailored Resume

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