(CW) Data Scientist
Novato, CA
Experience: 0
Category: Scientific & Clinical
Contractor Work Model: Remote
Brand: Joulé
Shift: On-Site
Compensation Range: 70.00 - 80.00 Per Hour
Job ID: 344831
Date Posted: 01/12/2026
Shortcut: http://jobs.systemone.com/nkuA3e
Job Title: Data Scientist, RBQM (Clinical Trials)
Location: Novato, CA
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
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Implement and maintain pre-defined KRIs, QTLs, and triggers using scalable SAS programs and macros across clinical studies.
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Extract, transform, and integrate data from EDC systems and other clinical data sources into analysis-ready datasets.
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Produce routine and ad hoc RBQM and central monitoring outputs, including tables, listings, extracts, and dashboard feeds.
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Perform quality control, validation, and troubleshooting of SAS programs to ensure accuracy and efficiency.
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Maintain technical documentation, including specifications, validation records, and change logs.
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Collaborate with Central Monitoring, Data Management, Biostatistics, and Study Operations to clarify requirements and ensure correct implementation of RBQM metrics.
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Support data-driven signal detection and study oversight activities throughout the clinical trial lifecycle.
Qualifications
Must Have
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PhD, MS, or BA/BS in statistics, biostatistics, computer science, data science, life sciences, or a related field.
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Relevant clinical development experience (programming, RBM/RBQM, or Data Management):
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PhD: 3+ years
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MS: 5+ years
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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
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Experience with RAVE EDC.
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Working knowledge of CDISC standards, including CDASH and SDTM.
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Exposure to R, Python, or JavaScript.
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Experience with clinical data visualization tools or platforms.
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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
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