Bayside Solutions

Statistical Programming Consultant

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is a Statistical Programming Consultant for a W2 contract lasting unspecified duration, with a pay rate of $166,400 - $187,200 per year. Located remotely, it requires 5+ years of clinical trial data analysis experience and expertise in SAS and CDISC standards.
🌎 - Country
United States
πŸ’± - Currency
$ USD
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πŸ’° - Day rate
720
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πŸ—“οΈ - Date
December 4, 2025
πŸ•’ - Duration
Unknown
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🏝️ - Location
Remote
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πŸ“„ - Contract
W2 Contractor
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πŸ”’ - Security
Unknown
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πŸ“ - Location detailed
United States
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🧠 - Skills detailed
#ADaM (Analysis Data Model) #Programming #CDISC (Clinical Data Interchange Standards Consortium) #Data Science #Datasets #Base #Compliance #Computer Science #Data Management #Mathematics #SQL (Structured Query Language) #Data Analysis #Statistics #SAS
Role description
Statistical Programming Consultant W2 Contract Salary Range: $166,400 - $187,200 per year Location: Redwood City, CA - Remote Role Job Summary: The Statistical Programmer will work with the Director or Senior Manager of Statistical Programmers and is responsible for assisting in the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Clinical Programming, Data Management, Biostatistics, Clinical Science, Medical Writing, Regulatory Publishing, and Development Operations. Duties and Responsibilities: β€’ Creates SAS programs to develop and/or validate SDTM datasets, ADaM datasets, and TFL outputs according to CDISC and internal standards. Ensures regulatory compliance and maintains traceability. β€’ Collaborates with colleagues to ensure high-quality deliverables. Works with vendors and β€’ Vendor oversight, as needed. β€’ Reviews and supports the development of programming specifications and annotated CRFs. β€’ Adopts a strategic approach to producing analytical deliverables, incorporating innovative tools and methods where needed. β€’ Contributes to standards, tools, and processes that improve the efficiency of producing analytics across programs. Requirements and Qualifications: β€’ BS or MS preferably in Data Science-related fields (e.g., Statistics, Mathematics, Epidemiology, Health Economics, Computer Science, Bioinformatics, etc.). β€’ Minimum of 5 years of experience in the analysis of clinical trial data. β€’ Must be experienced in the use of Base SAS, SAS Macro, SAS/STAT, SAS/Graph, SAS/SQL, and SAS/ODS. β€’ Must be experienced with CDISC standards. β€’ Submission experience preferred Desired Skills and Experience SAS programming, Base SAS, SAS Macro, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS, SDTM, ADaM, TFL generation, CDISC standards, statistical programming, clinical trial data analysis, data management collaboration, biostatistics collaboration, clinical science collaboration, medical writing collaboration, regulatory publishing collaboration, development operations collaboration, programming specifications, annotated CRFs, regulatory compliance, traceability, vendor oversight, analytical deliverables, innovative analytical tools, process improvement, data science, statistics, mathematics, epidemiology, health economics, computer science, bioinformatics, clinical data standards, submission experience Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com.