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Tier-1 employer and metro location with mid-level seniority create moderate competition.
Clinical SAS statistical programming requires industry-specific trial knowledge, making background fit highly sensitive.
Explicit 6+ years requirement and mandatory SAS/statistics skills raise shortlisting strictness.
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Lead development and maintenance of statistical programming solutions including programming, testing, and documentation for statistical tables, figures, and listings.
Plan and execute integration and quality control of analysis databases, and develop new process technologies, macros, and applications.
Act as a statistical team lead for individual studies including managing scope, resource forecasting, and providing training and guidance to junior staff.
Master's or Bachelor's Degree in Computer Science or related field, or equivalent combination of education, training, and experience.
At least 6 years of relevant experience in statistical programming or related domain.
Strong knowledge of statistics, clinical drug development processes, and proficiency in Base SAS, SAS/STAT, and SAS Macro Language.
Work Experience Required: Minimum 6+ years relevant experience.
Experienced in independently managing single-study statistical programming projects including scope and budget management.
Demonstrates advanced technical expertise to deliver project-related solutions and process improvements.
Capable of leading and training junior staff with strong organizational and communication skills.