[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Takeda Pharmaceutical jobs](https://jobs.opennash.com/companies/takeda-pharmaceutical/) · [Search jobs](/search/) Takeda Pharmaceutical # Manager, Clinical Data Scientist - Statistics Bhartiya City, Bengaluru, Karnātaka, India Full-time Manager or lead {'@type': 'MonetaryAmount', 'currency': 'USD', 'value': {'@type': 'QuantitativeValue', 'unitText': ''}} Data & Analytics Listed on Takeda Pharmaceutical’s official careers site. Posted October 14, 2026. Check that it is still open and apply there. [Apply on Takeda Pharmaceutical’s careers site →](https://jobs.takeda.com/job/bengaluru/manager-clinical-data-scientist-statistics/1113/101947656384) [OpenNash Jobs](https://jobs.opennash.com/) / [Takeda Pharmaceutical](https://jobs.opennash.com/companies/takeda-pharmaceutical/) / Manager, Clinical Data Scientist - Statistics ## Job description By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. ### Job Description Objective / Purpose: Describe at the highest level the team where this job sits and how this role will contribute to the team’s delivery of critical function. - Serve as a Manager-level Clinical Data Scientist within Data & Quantitative Sciences, applying statistical, data science, and analytical methods to support clinical development programs. - Contribute to cross-functional study teams by delivering analysis-ready data, quantitative analyses, visualizations, and interpretation summaries for assigned studies or workstreams. - Support fit-for-purpose statistical, data science, and advanced analytics activities under the direction of study and functional leadership. - Collaborate with cross-functional team members to support high-quality, traceable, analysis-ready, and submission-ready data. - Apply modern clinical data science practices, including automation, reusable analytics workflows, and approved AI/ML-enabled approaches, while maintaining scientific rigor, regulatory awareness, and patient-focused decision making. ### Accountabilities Primary duties and responsibilities; essential functions only. - Perform exploratory analyses, data visualization, and quantitative assessments using clinical trial, biomarker, external, and real-world data sources. - Apply established statistical, machine learning, simulation, and visualization methods to support interpretation of study results and development decisions. - Translate scientific and clinical questions into analysis-ready datasets, analysis specifications, and reproducible analytical workflows with guidance from senior team members. - Execute clinical data science activities for assigned studies or workstreams, ensuring timely delivery of high-quality analyses, data review, and quantitative insights that support study objectives. - Support integrated data review activities by identifying data trends, inconsistencies, and potential risks requiring further investigation. - Review and contribute to outputs produced by internal teams and external partners, ensuring adherence to established standards, processes, and quality expectations. - Communicate risks related to data quality, analytical assumptions, timelines, and quantitative outputs to study leadership and functional stakeholders. - Contribute to continuous improvement efforts through automation, reusable code, standard methodologies, and adoption of approved technologies and workflows. ### Education & Competencies (Technical and Behavioral) Essential and desirable education and competency requirements to perform the primary responsibilities of the job. Education / Experience - PhD in statistics, biostatistics, data science, epidemiology, biomedical engineering, computer science, quantitative sciences, or related field; or MS with 3+ years of relevant experience. Equivalent combinations should be reviewed with HR. - Experience contributing to quantitative analyses and data science activities within pharmaceutical, biotechnology, healthcare research, or other regulated clinical development environments. - Demonstrated ability to support clinical development decisions through quantitative analysis, data interpretation, and clear communication of evidence. - Experience working effectively on cross-functional study teams and collaborating across functional disciplines to achieve study objectives. - Experience working with clinical trial data and at least one additional data type such as biomarker, real-world, external, imaging, digital health, or other high-dimensional data sources. Highest-priority ### Technical Skills - Working knowledge of clinical trial design, drug development, endpoints, estimands, biomarkers, data interpretation, and the role of analytics in clinical decision making. - Solid foundation in statistics and quantitative methods, including longitudinal analysis, survival methods, causal reasoning, simulation, predictive modeling, and communication of uncertainty. - Ability to integrate, analyze, and interpret diverse data sources, including clinical trial, biomarker, real-world, external, imaging, digital health, or high-dimensional data as appropriate to assigned studies. - Practical understanding of AI/ML and advanced analytics in regulated clinical development, including model development, validation, documentation, assumptions, bias considerations, and fit-for-purpose deployment. - Hands-on proficiency in R and/or Python, with working knowledge of SAS and SQL; ability to develop and support reproducible analyses, code quality, version control, and validated workflows. - Ability to create clear analysis specifications, visualization approaches, documentation, and interpretation summaries suitable for scientific, operational, and study-team audiences. - Working knowledge of CDISC standards, including SDTM, ADaM, controlled terminology, Define-XML concepts, and submission-oriented data expectations. - Awareness of FDA, EMA, ICH-GCP, GxP, data privacy, inspection readiness, and traceability expectations relevant to clinical data and quantitative deliverables. - Familiarity with modern data platforms, reusable analytics workflows, automation, metadata-driven processes, and governed data standards. ### Behavioral Competencies - Communicates quantitative findings clearly to scientific, operational, technical, and study-team audiences. - Builds effective working relationships across study teams and functional partners. - Balances scientific rigor, quality, and timely delivery while proactively communicating risks and issues. - Demonstrates accountability for assigned deliverables and commitment to reproducible, traceable, high-quality work. - Demonstrates technical credibility, sound judgment, and collaborative problem-solving skills. - Embraces continuous learning and adoption of innovative analytical methods, automation, and AI-enabled approaches. Locations IND - Bengaluru - Research and Development Worker Type Employee Worker Sub-Type Regular Time Type Full time ## At a glance - Posted by the employer: Oct 14, 2026 - First seen by OpenNash: Oct 18, 2026 - Last checked: Oct 18, 2026 - Listed for: 4 days - Location: Bhartiya City, Bengaluru, Karnātaka, India - Employment type: Full-time - Pay: {'@type': 'MonetaryAmount', 'currency': 'USD', 'value': {'@type': 'QuantitativeValue', 'unitText': ''}}[Apply on Takeda Pharmaceutical’s careers site →](https://jobs.takeda.com/job/bengaluru/manager-clinical-data-scientist-statistics/1113/101947656384) ## More jobs at Takeda Pharmaceutical ### [Associate Director, Clinical Data Scientist - Statistics](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/c1566954193d1e5a1ad7/) Bhartiya City, Bengaluru, Karnātaka, India ### [Senior Manager, Clinical Data Scientist - Statistics](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/fcf8fb804a5ce9c19035/) Bhartiya City, Bengaluru, Karnātaka, India ### [Associate Director, Site Budgeting and Contracting](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/d8b4b66d202d69baa4b1/) Bhartiya City, Bengaluru, Karnātaka, India ### [VP Head, Site & Regional, Regulatory CMC – India.](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/cb609934be1cd1963b49/) Bhartiya City, Bengaluru, Karnātaka, India ### [Associate Director - Process Analytics Lead (US)](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/409650edfb20d7e5360b/) ## Similar jobs at other companies ### [Decision Scientist - Clinical Informatics (Clinical Data Standards)](https://jobs.opennash.com/companies/cvs-health/jobs/3549d29c96077c5c187a/) CVS Health ### [Manager, Clinical Data Scientist, Clinical Data Sciences](https://jobs.opennash.com/companies/pfizer/jobs/1fc3e30df8842360280e/) Pfizer · India - Chennai ### [Clinical Scientist](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/4d4d9107b85a316184b6/) Thermo Fisher Scientific · Shanghai, China ### [Clinical Scientist IRM - Lyon (h/f/nb)](https://jobs.opennash.com/companies/siemens/jobs/0b308c6e1c9b087f281d/) Siemens ### [DO NOT APPLY - TEST REQ - CRG - Specialist, Clinical Lab Scientist - Athlone Ireland](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/166617ba0eaee62b7f04/) Thermo Fisher Scientific · Athlone, Ireland OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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