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東京都の臨床開発・薬事の求人179件応募資格・募集要項・仕事内容を見る
Principal Statistician
掲載中・今日に確認
- 給与
- 記載なし
- 勤務地
- 東京都
- 休日
- 記載なし
- 雇用形態
- 記載なし
- ハイブリッド勤務
- 在宅勤務あり
どんな仕事かAIによる生成
Leads statistical planning and delivery for clinical research in Japan. The role covers trial design, analysis plans, interpretation of results, regulatory interactions, and collaboration with global and local teams.
この求人に応募
応募資格
必須
- Degree in statistics, biostatistics, mathematics or a closely related quantitative discipline.
- At least 5 years of experience working as a statistician in randomized clinical trials, with industry or CRO experience.
- Practical experience in clinical trial design and statistical analysis.
- Proficiency with statistical software such as R or SAS and working knowledge of clinical trial data formats and conventions.
- Business-level English and fluent Japanese (ability to read, write and speak in Japanese at professional level).
- Strong communication skills with experience explaining statistical concepts to non-statisticians.
歓迎
- PhD or advanced degree in statistics, biostatistics, or related field.
- Experience with regulatory submissions and direct interactions with Japanese regulatory authorities.
- Knowledge of adaptive designs, Bayesian methods, or other innovative statistical approaches.
- Background in one or more therapeutic areas relevant to our work in Japan.
- Experience managing external vendors and contract statisticians.
- Familiarity with data science tools and modern workflows oriented to reproducibility and automation.
求める人物像
- You bring strong statistical judgement and the ability to make clear recommendations.
- You enjoy working with diverse teams and communicating results in simple, actionable terms.
- You work with integrity and focus on patient impact.
- You welcome feedback and support the growth of others.
応募について
- We welcome applications from people with different backgrounds, experiences and perspectives.
募集要項最終確認 10/24
- 職種
- 臨床開発・薬事
- 雇用形態
- 記載なし
- 役職
- Principal Statistician
- 給与
- 記載なし
- 勤務地
- Japan - Tokyo - Akasaka
- 働き方
- This role is hybrid, based in Japan, combining on-site work with flexible remote days as agreed with the line manager.
- 経験年数
- 5年以上
- 選考の流れ
- Please submit your CV and a short cover note describing a statistical project you led and the impact it delivered.We will review applications and contact candidates for next steps.
- 掲載日
- 2026/10/23 15:03（1日前）
- 最終確認
- 2026/10/24 02:45（今日）
仕事内容
Position Summary
- You will lead statistical planning and delivery for clinical research in Japan. You will work with cross-functional teams to design trials, analyse data, and support regulatory interactions. We value clear scientific thinking, pragmatic problem solving, and a genuine focus on patients. You will grow technical and leadership skills while helping bring research advances to people who need them. Join us to use your statistical expertise to make a measurable difference and to develop your career in a supportive, mission-driven environment.
Responsibilities
- This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Act as the primary statistical lead for Japan projects, contributing to study design, analysis plans, and interpretation of results.
- Collaborate with global statisticians and local cross-functional teams to align trial design and analysis across regions.
- Prepare statistical input for regulatory interactions and support submissions to Japanese health authorities.
- Oversee external statistical partners and vendors to ensure quality, timelines, and cost control.
- Apply modern statistical methods, including adaptive and Bayesian approaches when appropriate, to enable efficient and ethical study designs.
- Coach and mentor statisticians and non-statistical colleagues, promoting good statistical practice and reproducibility.
この求人は、グラクソ・スミスクライン株式会社の採用ページの内容をAIが読み取って整理したものです。応募の前に採用ページの原文を確かめてください。データの集め方企業サイト
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