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Department/Team
Our chapter turns data into actionable insights to guide medical decisions and improve quality of life. We apply data management, data science, biostatistics and software development for preDCC, biomarker analysis, assay development, system integration, new technology such as mass spectrometry, clinical studies, PHC, the Cube, bioWARP, and more. Right now we work on more than 300 projects with collaborators across the entire Roche DIA.
Our contributions as an experienced partner for over 30 years, we apply our broad expertise in biostatistics and data science to create custom solutions in each phase of the diagnostic product lifecycle with a focus on Core Lab and Near Patient Care (NPC).
Your Key Responsibilities
Support all operational procedures to perform PHC clinical studies (including statistical programming, clinical/technical data management)
Support PHC clinical studies through management of clinical and technical databases, perform data handling and statistical programming, data integrity checks and reviews, ADS creation through the use of R programming language
Manage external business partners including Pharma partners to deliver their contributions globally by local follow-up
Support study managers globally to follow global data management procedures
Drive data standardization for clinical studies and ensure FAIR (findable, accessible, interoperable, and reusable) data principles are prioritized
Mediator for business processes to be shared between local Biostatistics and Data Management departments
Improve efficiency of data management procedures to allow for organizational agility and empowerment
Provide digital tools development support for study data standardization, analytics, data validation and ADS creation and to ensure quality of data for analysis and regulatory submission
Develop and Implement clinical digital solutions and AI models for data handling, data acquisition and monitoring (including data selection and merge from different data sources and ad-hoc reporting)
Who you are
Degree in Science or Medical Information (Informatics), with a strong preference for candidates holding a PhD and have experience in clinical trial management, medical documentation, biomedical engineering, neurology, bioinformatics, informatics, or biostatistics
Experience in Data Management (DM) and statistical programming, demonstrating a deep understanding of the field of data science
Demonstrated strong experience in managing clinical trials compliance and driving process management and improvements
Expertise in statistical software such as R or SAS, along with good knowledge of clinical study databases and SQL and AI/ML tools/methodologies. Proficient in process and project documentation
Experienced in working with international teams
You have a very strong knowledge in clinical databases, GxP standards, clinical chemistry, and diagnostic assays
Your expertise in statistics and project management is on a good level as well as fundamental understanding of medical terminology
Application documents
To make the application process as convenient as possible for you please add only your updated CV. References and certificates are not required at this stage.
We look forward to receiving your application!
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At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Roche at Penzberg, near Munich, employs more than 7,000 people. The site is one of the largest biotechnology centers in Europe and the only Roche site with research, development and production for both Pharmaceuticals and Diagnostics under one roof. From your beginning with Roche, our motivated team will welcome and support you. Numerous opportunities for personal development, flexible work hours, attractive compensation packages and special family assistance programs are available.
Roche is an Equal Opportunity Employer.