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Sr. Clinical Data Analyst (Contractor) (Office or Remote)
Arcus BiosciencesUnited StatesRemotefull_timeVerifiedPosted 17 Dec 2024
About the role
This is a full-time, one year contract role. The Sr. Clinical Data Analyst will be responsible for creating fit-for-purpose analyses, visual data displays and dashboards from diverse data types to aid in internal data consumption and decision-making. This position will report into the Head of Clinical Data Sciences and will interact regularly with diverse stakeholders across the organization. Demonstrated abilities to prioritize work; to understand internal business, data and decision-making needs; and to communicate and collaborate with key stakeholders both within Biometrics and beyond (research, translational science, clinical science, clinical operations, safety, medical affairs and commercial) are essential. This is a unique opportunity to join a growing Biometrics team investigating a diverse portfolio of immuno-oncology therapeutics. The ideal candidate will come with industry experience working in a regulated environment while also demonstrating know-how, flexibility and scientific curiosity to drive creative approaches to both formal and exploratory work. Responsibilities
- Generate validated, reproducible, visualizations and analysis using open-source software packages or tools (e.g., R/R-Shiny, Spotfire) to replicate more formal analyses for the purpose of clinical trial planning and design, internal data review, go/no-go decision-making and external publications or data releases
- Standardize and internalize current Spotfire and other Dashboards to provide semi-automation to full automation where appropriate
- Explore other open-source Data Science languages such as Python in fit-for-use analytical environment
- Develop and implement R programming such as standardized packages, functions, Markdown, Flex-dashboards, R-Shiny, etc in existing analytical pipelines and new pipelines including automation of standards
- Create integrated data analyses pooling data across various clinical trials or with other relevant data sources to meet business needs (e.g., real-world data analyses, tumor or indication-specific translational questions, site monitoring, safety signal detection, go/no-go decision-making), as appropriate
- Develop therapeutic area landscape and benchmark analyses to facilitate discussions on new target selection, clinical development and commercialization strategies
- Build and maintain data pipelines to automate data processing tasks
- Bachelor’s or Master’s degree in a data science field, e.g., statistics, mathematics, epidemiology, computer science, bioinformatics, or another field with commensurate levels of experience
- Minimum 4+ years of biotechnology or pharmaceutical experience, with (immuno-) oncology experience preferred
- Programming experience in R or Python or similar language is a must as is experience with data display and dashboard tools such as R-Shiny, Spotfire, and Tableau (or similar)
- Familiarity with reproducibility, traceability and containers (Docker) strongly preferred
- Knowledge of clinical CDISC data standards and associated requirements of working in validated environments strongly preferred
- Demonstrated ability to rapidly adapt to changing project and strategic requirements
- Interest in continuing education, particularly in the areas of business knowledge as well as technology trends for producing analyses and visualizations (particularly with an eye towards reproducibility or interactivity)
- Takes a fit-for-purpose mindset to daily work as well as long-term vision
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