Senior Statistical Programmer Analyst - T

Role overview Develop and review statistical programs and clinical trial datasets used in analysis and regulatory submissions. Working with statisticians, programmers, data managers, and other study partners, you’ll help ensure that clinical data is prepared, analyzed, documented, and handled in line with applicable standards and quality requirements. The role also provides subject matter guidance and mentoring to less experienced programmers.

Responsibilities - Translate specifications and statistical analysis plans into algorithms, analysis dataset specifications, and SAS programs. - Produce and independently check clinical data listings, summary tables, and graphs. - Import, export, clean, transform, and analyze study data, and support data management teams with edit checks. - Prepare trial datasets and programs for regulatory submission, maintaining alignment with relevant clinical data standards and electronic submission guidance. - Maintain and manage libraries of clinical study data, metadata, SAS code, and reusable macros. - Coordinate with statisticians, programmers, data managers, regulatory and quality staff, and external clinical system vendors; mentor colleagues and promote sound programming practices.

Requirements - Bachelor’s degree in statistics, computer science, or a related field, plus at least five years of statistical programming experience, including at least three years in clinical programming in a medical device or related life sciences setting; equivalent education and experience may be considered. - Strong SAS programming capability for data import and transformation, statistical procedures, reporting, and graphics. - Knowledge of clinical data standards and regulatory requirements for clinical databases and submissions. - Ability to manage multiple tasks with accuracy and close attention to detail. - Strong written, verbal, and interpersonal communication skills. - Proficiency with standard office software.

Nice to have - Familiarity with Base SAS, SAS/GRAPH, SAS/ODS, SAS/STAT, macro programming, and SAS/SQL; SAS programmer certification is preferred. - Knowledge of standards such as CDASH, SDTM, ADaM, ODM, Define, and controlled terminology. - Experience with metadata repositories, regulatory submissions, or clinical data management systems such as InForm or RAVE.

Benefits and work setup The position is based in a general office environment and involves approximately 10% travel to conferences or affiliated facilities. The stated hourly base pay range is $65–$115, with compensation varying by qualifications, skills, and work location. Eligible benefits include health and insurance coverage, a 401(k) match, paid parental leave, paid holidays, vacation, and sick time.