Senior Expert I

Directly involved in the development and maintenance of the LIMS, pipeline, and assays - with the goal of producing high-quality, analyzable datasets - both reported to the clinical trial teams and used for additional research (bed-to-bench / back-translation) activities to answer our key scientific questions. Duties include: Design, development, maintenance, and support of the NGDx LIMS, pipeline framework, pipelines and assays, including Quality Control (QC) - current codebase is a combination of Java, Python, and R Work with various partners from lab associates to clinical trial data management in the development of assays to support our trials and additional research Implementing robust tooling for the development of new assays and the integration of new data types from CROs and collaborations Maintaining consistent support for data generation and ingestion / QC activities Enabling analysts to concentrate on subject matter expertise and analytics crucial for new assay development, as well as facilitating effective communication with clinical teams for data interpretation support Become a subject matter expert in our various Novartis data science platforms / tooling in order to support other OncDS analysts Coordinate, as needed, with Novartis IT as a bridge with Oncology leveraging your engineering expertise

5 years of work experience in the job offered or related position. Requires experience with:

experience with the following:

• Developing, implementing and delivering data products, data strategies, data governance frameworks, and data quality standards, relevant to clinical applications
• Working with diverse and large-scale clinical data sources, such as clinical trials, real-world data, genomics, imaging, and digital health