What are the responsibilities and job description for the Senior Data Scientist II, Real World Evidence position at Tempus AI?
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
The Real World Evidence (RWE) group within the Pharma R&D team at Tempus works with pharmaceutical partners to provide best-in-class data, analysis, and methodological guidance to Tempus’s real-world data offering. We are seeking a highly motivated and solutions-oriented Sr. Data Scientist II, RWE with experience and interest in oncology and clinical / epidemiological study design and execution to join our team. Top candidates will have experience working with observational healthcare or clinical trial data, and expertise in biostatistics, epidemiology, and / or real-world data analytics.
Responsibilities :
- Spearhead analyses of Tempus data for RWE studies in collaboration with major pharmaceutical partners.
- Advance Tempus' offerings to pharmaceutical partners by leading projects that incorporate cutting-edge machine learning and artificial intelligence techniques.
- Execute advanced coding and derive real-world endpoints, demonstrating a deep understanding of Tempus' molecular and clinical datasets.
- Provide mentorship to junior colleagues on technical skills, fostering their professional growth and enhancing team capabilities.
- Analyze and interpret RWE study results to draw appropriate inferences, considering study design and statistical methodologies, while also assessing study limitations.
- Articulate research findings to external Pharma partners' RWE and clinical teams, offering strategic insights and recommendations.
- Collaborate with internal teams, including engineering, oncology, bioinformatics, and clinical abstraction, to continuously improve Tempus data quality, products, and analytical best practices.
- Stay on top of the latest methodological advancements in real-world studies and oncology guidelines (NCCN and ongoing clinical trials), ensuring alignment with the evolving oncology landscape within Tempus’ database.
- Ensure compliance with all relevant regulations and company procedures.
Minimum Qualifications :
Beneficial :
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