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| 部署・役職名 | Principal Data Scientist/Non－Line Manager, Experimental Medicine Japan D＆A |
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| 仕事内容 |
【Basic Purpose of the Job】 Supports the complete clinical/pharmaceutical drug lifecycle process （research, development, market access, and market supply） through: ・Strategic planning and execution ・Data transformation ・Descriptive analytics ・Diagnostic analytics ・Predictive analytics ・Prescriptive analytics Works with data from: ・Clinical trials ・Clinical registries ・Real－world databases Provides: ・Analytics tools ・Data outputs ・Scientific insights and inference May act as an ExpMED Product Owner up to the substance/asset level and represent ExpMED on data science－related matters. 【Key Accountabilities】 Data Science Leadership Responsible for: ・Leading and overseeing design, transformation, analysis and reporting for complex Phase I－IV clinical trials ・Supporting complex international projects ・Leading analysis of registry and real－world data ・Delivering data science solutions aligned with specific project and asset needs Success Measures ・Quality deliverables ・Timeline adherence ・Feedback from development teams, Product Owners and capability managers 【Innovation ＆ Scientific Advancement】 ・Stay current on developments in data science both within and outside BI ・Convert insights into new data science approaches supporting: －Discovery －Clinical development －Regulatory registration －Manufacturing －Commercialization Success Measures ・Quality of innovative solutions ・Adoption of new processes and tools ・Stakeholder feedback 【Data Storytelling ＆ Communication】 ・Present compelling, validated stories based on complex data science findings ・Communicate effectively with scientific and non－scientific stakeholders Success Measures ・Quality and frequency of presentations ・Audience understanding and feedback 【Compliance ＆ Data Quality】 ・Ensure data transformation and analysis specifications are: －Complete －Accurate －SOP－compliant －GxP－compliant Success Measures ・Regulatory acceptance ・Quality of specifications 【Coaching ＆ Knowledge Sharing】 ・Guide and lead colleagues ・Support internal customers and external partners ・Promote knowledge sharing within the Clinical Data Science community Success Measures ・Feedback from colleagues ・Increased knowledge sharing and capability development 【Cross－Functional Leadership】 ・Participate in BI cross－functional working groups ・Lead One Human Pharma internal working groups ・Participate in external industry working groups ・Drive relevant data science initiatives Success Measures ・Quality of leadership ・Business impact of working group outcomes ・Feedback from Global Product Owners and Product Owners 【Product Owner Responsibilities】 Where applicable: ・Support the clinical drug lifecycle process as an ExpMED Product Owner ・Provide leadership at product, substance and asset level Success Measures ・Product quality ・Leadership effectiveness ・Timeline adherence ・Stakeholder satisfaction 【Collaboration ＆ Digital Innovation】 ・Promote cross－functional teamwork within ExpMED and across BI ・Support innovative digital solutions ・Drive predictive models and intelligent optimization approaches ・Contribute to organization－wide innovation initiatives Success Measures ・Quality of collaboration ・Frequency of innovative digital initiatives ・Stakeholder feedback 【Regulatory ＆ Organizational Requirements】 Must understand and implement: Regulatory Requirements ・International Good Clinical Practice （GCP） ・Good Statistical Practice ・ICH guidelines and regulations across all regions Clinical Development Requirements ・Statistical methodology guidance ・Clinical development standards ・Therapeutic Area－specific requirements Internal Requirements ・BI processes ・Standard Operating Procedures （SOPs） ・Clinical Development Plan requirements Additional Requirements （where applicable） ・Good Laboratory Practice （GLP） ・Good Manufacturing Practice （GMP） 【Job Complexity】 ・Solves complex, defined problems ・Has strategic impact across the clinical drug lifecycle ・Considers the needs and requirements of multiple departments and stakeholders ・Influences decision－making at a broader organizational level 【Interfaces】 Collaborates with: ・GCO ・GPV ・Therapeutic Areas ・TMCP ・GRA ・Research ・Development ・Pharma Supply Represents BI regarding: ・Clinical planning ・Data transformation ・Statistical analyses ・Critical regulatory requests ・Project and asset－level data science activities 【Job Impact】 Responsible for: ・Analysis of clinical drug lifecycle data ・Delivering scientific insights to internal and external stakeholders ・Independent decision－making related to data science activities ・Translating data into business and scientific value ・Results must be tailored to customer and stakeholder needs. |
| 労働条件 |
契約期間：期間の定めなし 試用期間：あり（3カ月） 就業時間：8:45～17:20（うち休憩45分間） 休日：土日、祝日 その他各種会社休日あり（年間127日：2025年） 休暇：年次有給休暇（入社初日に6～16日を付与）、慶弔休暇・リフレッシュ休暇等各種有休特別休暇制度あり 残業：あり 給与改定：年1回（4月） 通勤手当：会社規定に基づき支給 社会保険：健康保険、厚生年金、労災保険、雇用保険 |
| 応募資格 |
【必須（MUST）】 【Experience ＆ Expertise】Required: Data Science Expertise ・Strong understanding and application of data science principles ・Broad expertise in: ・Planning analyses ・Data transformation ・Statistical analysis ・Interpretation of results ・Reporting Technical Expertise ・Broad knowledge and advanced experience in relevant programming/software languages Clinical Development Expertise ・Advanced understanding of the clinical drug development lifecycle ・Strong understanding of clinical trial development Leadership ・Advanced project leadership experience required Experience Requirements ・PhD: 3＋ years in pharmaceutical industry, CROs, regulatory authorities, or academia ・MSc: 6＋ years in pharmaceutical industry, CROs, regulatory authorities, or academia ・Bachelor's Degree: 7＋ years of data science experience Deep subject matter expertise may partially compensate for experience requirements. Education Requirements Bachelor's, Master's or Doctoral degree in: ・Statistics ・Mathematics ・Computer Science ・Data Science ・Psychology ・Finance ・Related quantitative disciplines 【Required Capabilities】 Statistical ＆ Scientific Expertise ・Thorough knowledge of statistical methodology ・Strong understanding of experimental design and clinical trials ・Understanding of terminology related to supported disease areas and assets ・Experience processing clinical trial information Advanced Analytics ・In－depth understanding of advanced statistical concepts used in Data Science Technical Skills ・Advanced working knowledge of multiple relevant Leadership ＆ Training ・Ability to lead and facilitate meetings ・Ability to develop and deliver data science training ・Strong project leadership capability Communication ・Fluent English （Read / Write / Speak） ・Strong communication and presentation skills Collaboration ・Proven ability to work within global and remote teams ・Strong stakeholder management skills ・Effective collaboration with CROs, experts and management Problem Solving ・Proactively identify issues ・Develop solutions ・Interact independently with internal and external stakeholders on data science matters Cultural Awareness ・Effective communication across local and global cultures ・Sensitivity to internal and external stakeholder needs 【Quick Candidate Snapshot】 ・PhD ＋ 3 years, MSc ＋ 6 years, or Bachelor's ＋ 7 years of relevant Data Science experience ・Strong statistical analysis and programming expertise ・Experience with clinical trial, registry and/or real－world data ・Strong understanding of pharmaceutical R＆D and clinical development ・Advanced project leadership experience ・Experience driving innovation and digital transformation ・Strong stakeholder management and data storytelling capabilities ・Fluent English communication skills |
| リモートワーク | 可 「可」と表示されている場合でも、「在宅に限る」「一定期間のみ」など、条件は求人によって異なります |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2026/07/15 |
| 求人番号 | 9136345 |
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