• (CW) Data Scientist

    System One (Novato, CA)


    Job Title: Data Scientist, RBQM (Clinical Trials)

    Hours/Schedule: Monday–Friday, 8 am to 5 pm

    Compensation: $72.00–$79.00 hourly, DOQ

     

    Type: Contract

     

    We cannot work C2C with any other agency - must be US based

    Overview

    The Data Scientist, RBQM supports central monitoring and risk-based quality management activities for clinical trials by delivering robust, SAS-driven analytics across multiple studies. This role partners closely with Data Management, Biostatistics, and Clinical Operations to implement key risk indicators and ensure high-quality, analysis-ready clinical data.

    Responsibilities

    + Implement and maintain pre-defined KRIs, QTLs, and triggers using scalable SAS programs and macros across clinical studies.

    + Extract, transform, and integrate data from EDC systems and other clinical data sources into analysis-ready datasets.

    + Produce routine and ad hoc RBQM and central monitoring outputs, including tables, listings, extracts, and dashboard feeds.

    + Perform quality control, validation, and troubleshooting of SAS programs to ensure accuracy and efficiency.

    + Maintain technical documentation, including specifications, validation records, and change logs.

    + Collaborate with Central Monitoring, Data Management, Biostatistics, and Study Operations to clarify requirements and ensure correct implementation of RBQM metrics.

    + Support data-driven signal detection and study oversight activities throughout the clinical trial lifecycle.

    Qualifications Must Have

    + PhD, MS, or BA/BS in statistics, biostatistics, computer science, data science, life sciences, or a related field.

    + Relevant clinical development experience (programming, RBM/RBQM, or Data Management):

    + PhD: 3+ years

    + MS: 5+ years

    + BA/BS: 8+ years

    + Advanced SAS programming expertise in a clinical trials environment (Base SAS, Macro, SAS SQL).

    + Hands-on experience working with large, complex clinical trial datasets.

    + Proficiency with Microsoft Word, Excel, and PowerPoint.

    Nice to Have

    + Experience with RAVE EDC.

    + Working knowledge of CDISC standards, including CDASH and SDTM.

    + Exposure to R, Python, or JavaScript.

    + Experience with clinical data visualization tools or platforms.

    + Knowledge of GCP, ICH, and FDA guidance related to clinical trials and risk-based monitoring.

     

    Benefits

     

    System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.

     

    Ref: #568-Clinical

     

    System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

     

    System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.