Data Scientist

Data Scientist – RBQM Work Location: Fully Remote Job Title: Data Scientist - RBQM Pay Rate: Up to $76/hour DOE Contract: 3-month assignment with potential to extend or convert We’re partnering with a leading biotechnology organization to find a Data Scientist with strong SAS programming experience to support Risk-Based Quality Management (RBQM) and centralized monitoring for clinical trials. This is a contract opportunity (initial 3 months) with potential for extension or conversion, supporting multiple clinical studies in a fast-paced, data-driven environment. Key responsibilities: • Implement and maintain Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and risk triggers across multiple clinical studies • Develop, run, and maintain robust SAS programs and macros (Base SAS, SAS SQL, Macros) • Extract, transform, and integrate data from EDC systems (e.g., RAVE) and other clinical data sources • Produce routine and ad-hoc centralized monitoring outputs, including tables, listings, data extracts, and dashboard feeds • Perform QC, validation, and troubleshooting of SAS code to ensure accurate and efficient outputs • Maintain technical documentation such as specifications, validation records, and change logs • Collaborate closely with Data Management, Central Monitoring, Biostatistics, and Clinical Operations teams Required qualifications: • Degree in Statistics, Biostatistics, Data Science, Computer Science, Life Sciences, or a related field • Relevant clinical development experience aligned to education level: • PhD with 3+ years • MS with 5+ years • BA/BS with 8+ years • Advanced SAS programming experience in a clinical trials environment (hard requirement) • Hands-on experience working with large, complex clinical trial datasets • Proficiency with Microsoft Word, Excel, and PowerPoint • Knowledge of GCP, ICH, and FDA guidance related to clinical trials and risk-based monitoring Preferred / strong plus: • Experience with RAVE EDC • Familiarity with CDISC standards (SDTM, CDASH) • Exposure to R, Python, JavaScript, and/or clinical data visualization tools • Prior experience supporting RBQM, RBM, or centralized monitoring activities Role details: • Contract length: 3 months (potential extension or conversion) • Location: Remote / Offsite • Focus: Clinical trial analytics, centralized monitoring, RBQM