Senior Clinical Data Scientist

Summary

Join N-Power Medicine as a Senior Clinical Data Scientist and play a pivotal role in supporting clinical trial analysis and reporting. You will develop, validate, and maintain SAS and/or R programs, extract and transform clinical data, and create analysis datasets for pharmaceutical partners. Responsibilities include applying CDISC standards to ensure compliant datasets, collaborating with various teams, performing quality checks, and generating reports. This fully remote position within the United States offers the opportunity to contribute to a mission-driven company focused on accelerating better therapies for patients. The Statistical Programming & Analysis team collaborates with Clinical Science, Quantitative Sciences, and Network Services teams. You will be responsible for delivering status reports, tables, listings, figures, and analysis datasets.

Requirements

• Bachelor’s degree required; Master’s degree in a related field (e.g., Public Health, Biostatistics, Health Informatics, Computer Science) strongly preferred
• 5+ years of experience in healthcare data analysis, with a strong focus on clinical trials and/or real-world data and oncology studies
• Proficiency in SAS Analytics, including SAS macro programming and advanced procedures
• Solid working knowledge of CDISC data standards (SDTM, ADaM)
• Demonstrated ability to communicate complex analytical findings clearly and effectively to diverse audiences, including clinical operations, medical directors, and senior executives
• Demonstrated ability to co-develop or implement statistical analysis plans for prospective clinical trials
• Excellent technical, analytical, written, and verbal communication skills

Responsibilities

• Develop, validate, and maintain SAS and R programs to support clinical trial data analysis and reporting
• Create, write, and verify SAS programs for data listings, metrics, and reconciliation reports following departmental QA procedures
• Extract and transform data from various database sources to create analysis datasets as specified by pharmaceutical clients
• Provide summary, analysis, tables, listings and figures (TLF) or other deliverables for clients or network partners per study protocol
• As needed, serve as SDTM programmer across multiple studies, ensuring timely and accurate SDTM dataset creation per protocol
• Apply CDISC guidelines in the development of SDTM and ADaM-compliant datasets, ensuring industry-standard compliance
• Collaborate with Quantitative Sciences (Biostatistics) and Clinical Science teams to create data specifications, draft or review statistical analysis plans (SAP)
• Collaborate with upstream data sources, Software Engineering, and Clinical Informatics teams to identify and extract prescreening data for ongoing studies and feasibility assessments
• Perform routine data validation checks and generate clinical data review listings to support Clinical Operations and Abstraction teams in ensuring data accuracy and completeness
• Provide study-specific metrics and status reports (e.g., coding metrics, drug dispensation metrics, subject status reports), and TLFs for abstracts, conferences or publications
• Perform other duties as assigned to support team and company goals

Preferred Qualifications

• Familiarity with clinical coding systems (e.g., ICD, LOINC, RxNorm, MedDRA, WHO-Drug) and their use in clinical trial setting analysis is preferred
• Experience interpreting and analyzing EHR, claims or other real world data (RWD) is a plus

Benefits

• The expected salary range for this position is $150,000 and $185,000
• Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law
• N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performance
• This position is eligible for company benefits
• 401K plan