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Protocol Intelligence
Data-driven signals on your job's competitivenessGlobal brand plus mid-level SAS programmer role, but niche clinical-statistics skillset limits broad applicant pool.
High — clinical trial SAS programming and statistical analysis skills are highly domain-specific to pharma/biotech.
High — explicit years plus mandatory SAS/SAS-STAT/Macro and clinical statistics experience required.
Job Description
Structured overview of role & requirementsAbout This Role
Develop, test, and document programs to create statistical tables, figures, and listings for clinical study data.
Lead programming tasks including creating analysis databases, performing QC checks, and integrating data from multiple studies.
Provide technical expertise, lead single study projects under supervision, manage scope of work, and provide training to junior staff.
Minimum Requirements
Master's degree in Computer Science or related field with 4 years relevant experience, OR Bachelor's degree with 5 years relevant experience, OR equivalent combination of education, training, and experience.
Proficient in Base SAS, SAS/STAT, and SAS Macro Language programming.
Knowledge of statistics, programming, and clinical drug development process.
Work Experience Required: 4-5 years relevant experience depending on degree.
Ideal Candidate Profile
Experienced in statistical programming within clinical research environment with ability to plan and lead portions of projects independently.
Strong understanding of clinical drug development and ability to estimate workload, manage scope, and forecast resources for single studies.
Skilled at mentoring and training junior programmers while maintaining high accuracy and detail orientation.