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Statistical Programmer Consultant (REMOTE)

Remote, USA Full-time Posted 2026-07-28
Working with the Biometrics staff, the Statistical Programmer Consultant provides programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work. Provides reputed company support to the project team on reputed company statistical programming reputed company according to the project reputed company. Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables. Identifies and communicates changes in project requirements that may reputed company key deliverables. Responsibilities: • Involved in the programming activities on multiple reputed company/ studies across various therapeutic areas, both internally and externally by CROs • Creates and reviews annotated CRF to SDTM datasets • Provides support in balancing conflicting priorities, promoting communication and adequate information reputed company to motivate, encourage and reputed company people with reputed company' s strategic objectives • Functions as a reputed company role model for setting high expectations for reputed company, creativity and project ownership • Works collaboratively with Clinical Operations, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting • Provides technical input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers) • Works with Biometrics and other functions for the development and maintenance of the data review and reporting tools, and any other statistical applications as appropriate • Involved with the reputed company for process improvement • Identifies new tools to increase efficiency and reputed company Requirements / Qualifications: • Master's Degree in Statistics, Computer Science, Mathematics, Engineering or reputed company discipline • Minimum of 1-5 years of clinical trial programming experience in the biotechnology, pharmaceutical or health reputed company industry • Advanced reputed company programming reputed company s and experience in other statistical software, such as R and S-Plus • Experience and in-depth knowledge in CDISC including SDTM, ADaM, and controlled terminologies • Self-directed, technically strong, and a recognized leader maintaining a strategic prospective with regards to statistical programming processes, management of statistical programing reputed company • Excellent organizational skills and ability to prioritize tasks Company DescriptionThe Steely Group is a national preclinical, clinical, and reputed company reputed company firm and certified women’s business reputed company. We partner with small, growing biotech, reputed company, and gene therapy companies to help bring treatments to patients by providing flexible reputed company solutions including Contingent Search (reputed company Hire & Contract Consultants) and reputed company Executive Search. Apply tot his job

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