> Markdown version of [/jobs/ext/4081106-clinical-data-scientist](https://www.wearedevelopers.com/jobs/ext/4081106-clinical-data-scientist). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Clinical Data Scientist - **Company:** Boehringer Ingelheim GmbH - **Location:** Biberach, Germany - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Artificial Intelligence, Clinical Data Management, Clinical Data Repository, R (Programming Language), SAS (Software), Information Technology, Performance Monitor - **Published:** October 22, 2026 - **Apply:** https://dejobs.org/x/x/CACD9F2BE76F43B0A900752DB0790667/job/ ## About the Role and advanced statistical methods to improve efficiency and scalability. + Finally, you will generate actionable insights from clinical data through visualization and contribute to evidence-based decision-making across the value chain. + You coordinate dependencies, priorities, risks, and timelines across assigned studies and projects, ensuring transparent communication, effective collaboration with multidisciplinary experts, and reliable delivery. **Requirements** + Bachelor of Science (BSc) or Master of Science (MSc) in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc). + Several years of data science experience in pharmaceutical development and statistical programming for clinical trials, particularly with SAS and R (working experience might be partially compensated by broad and deep topic-specific knowledge). + Sound knowledge of CDISC standards, statistical methodology, clinical trial design, medical terminology, and clinical trial data processing. + Practical understanding of AI-enabled solutions and automation, including responsible, compliant, and value-adding use in clinical data science. + Strong organizational and coordination skills, with the ability to manage multiple activities, interfaces, dependencies, priorities, and timelines in a global, cross-functional environment. + Experience in vendor governance and CRO oversight, including expectation setting, performance monitoring, quality review, issue management, escalation, and pragmatic problem-solving. + Strong English communication and interpersonal skills, a collaborative and agile mindset, and the ability to explain complex data science concepts clearly; experience with agile teams or as a product owner is an advantage. Start date: 01.01.2027/ asap Apply until: **November 5** **th** **, 2026** As part of our commitment to transparency and fairness, salary information will be shared during the recruitment process. We also offer a, Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients, and communities. All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law ## Description all aspects of descriptive, diagnostic, predictive and prescriptive analytics of data. This position can either be filled in Ingelheim or Biberach. **Tasks & responsibilities** + You independently plan, conduct, and coordinate statistical programming activities for assigned clinical trials and projects, including data transformation, statistical analyses, and the delivery of high-quality reports and outputs. + In addition, you design, program, validate, and maintain CDISC-compliant datasets and associated deliverables, supporting the delivery of complete, consistent, and submission-ready data for assigned studies and stakeholder needs. + Moreover, you will coordinate and oversee CROs and external partner contributions, ensuring quality, progress, and risk mitigation. + The duties will also include the collaboration with cross-functional stakeholders to translate scientific and business needs into data-driven solutions. + Furthermore, you'll drive innovation through AI, automation, R, senior-clinical-data-scientist-with-a-focus-on-statistical-programming/jobs-in::Senior Clinical Data Scientist with a Focus on Statistical Programming