Joulé
(CW) Data Scientist
⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Data Scientist, RBQM in Novato, CA, on a contract basis for an hourly pay of $72.00–$79.00. Requires a PhD/MS/BA in relevant fields, advanced SAS skills, and clinical development experience.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
632
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🗓️ - Date
January 13, 2026
🕒 - Duration
Unknown
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🏝️ - Location
On-site
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📄 - Contract
W2 Contractor
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🔒 - Security
Unknown
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📍 - Location detailed
Novato, CA
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🧠 - Skills detailed
#CDISC (Clinical Data Interchange Standards Consortium) #"ETL (Extract #Transform #Load)" #Visualization #Data Science #SQL (Structured Query Language) #Datasets #Base #GCP (Google Cloud Platform) #Data Management #Python #R #Computer Science #Statistics #Monitoring #Macros #Documentation #Triggers #Scala #JavaScript #SAS #Programming
Role description
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
• 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.
QualificationsMust 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
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
• 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.
QualificationsMust 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
