Largeton Group ยท 1 week ago
RBQM Data Scientist
United States
Full-time
Remote
Mid Level
$70/hr - $75/hrLargeton Group is seeking an RBQM Data Scientist to support central monitoring and risk-based quality management for pharmaceutical clinical trials. The role involves implementing key risk indicators, extracting and integrating clinical data, and collaborating with cross-functional teams to ensure effective RBQM metrics.
ConsultingInformation TechnologyTraining
Responsibilities
Support central monitoring and risk-based quality management (RBQM) for pharmaceutical clinical trials
Implement and maintain pre-defined Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and triggers using advanced SAS programming
Extract, transform, and integrate clinical data from EDC systems (e.g., RAVE) and other sources into analysis-ready SAS datasets
Generate routine and ad-hoc RBQM/central monitoring outputs (tables, listings, data extracts, dashboard feeds) for signal detection and study review
Perform quality control and troubleshooting of SAS code to ensure accuracy and efficiency of outputs
Maintain thorough technical documentation for all RBQM programs and processes, including specifications, validation records, and change logs
Collaborate with cross-functional teams (Central Monitors, Statistical Monitors, Data Management, Biostatistics, Study Operations) to gather requirements and implement RBQM metrics correctly
Utilize strong pharmaceutical clinical development experience and advanced SAS skills in a clinical trial setting
Qualification
Required
Support central monitoring and risk-based quality management (RBQM) for pharmaceutical clinical trials
Implement and maintain pre-defined Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and triggers using advanced SAS programming
Extract, transform, and integrate clinical data from EDC systems (e.g., RAVE) and other sources into analysis-ready SAS datasets
Generate routine and ad-hoc RBQM/central monitoring outputs (tables, listings, data extracts, dashboard feeds) for signal detection and study review
Perform quality control and troubleshooting of SAS code to ensure accuracy and efficiency of outputs
Maintain thorough technical documentation for all RBQM programs and processes, including specifications, validation records, and change logs
Collaborate with cross-functional teams (Central Monitors, Statistical Monitors, Data Management, Biostatistics, Study Operations) to gather requirements and implement RBQM metrics correctly
Utilize strong pharmaceutical clinical development experience and advanced SAS skills in a clinical trial setting
Education requirements: PhD/MS/BA/BS in relevant field with appropriate years of clinical development experience
Preferred
Prefer candidates with experience in RAVE EDC, knowledge of CDISC standards, and exposure to other programming languages or clinical data visualization tools
Company
Largeton Group
At Largeton Group, we're passionate about empowering businesses to reach new heights through innovative staffing solutions and cutting-edge technology.
Founded in 2014
51-200 employees
H1B Sponsorship
Largeton Group has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (5)
2024 (10)
2023 (8)
2022 (6)
2021 (7)
2020 (11)
Funding
Current Stage
Growth StageLeadership Team
Ashutosh Tripathi
Managing Partner
Saurabh Prakash
Client Partnership Manager.
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