Senior Statistical Programmer

Qualifications and Skills:

• Required qualifications:
• Bachelor’s or Master’s degree in a relevant technical field (e.g., statistics, computer science, mathematics, data science, or epidemiology) and a minimum of 5 years of statistical programming experience in clinical research.
• Advanced proficiency in statistical programming (SAS or R; SAS preferred), including complex analysis datasets and TLFs.
• Familiarity with clinical data standards (CDISC, including SDTM and ADaM).
• Working knowledge of statistical methods used in clinical trials, sufficient to contribute to analysis planning and to interpret outputs.
• Strong understanding of TLF structure and clinical study data.
• Ability to work independently and manage multiple deliverables and deadlines within a cross-functional team.
• Strong attention to detail and a quality-control mindset, including review of others’ work.
• Good written and verbal communication skills.
• Preferred qualifications:
• Experience producing TLFs for clinical study reports or regulatory submissions.
• Familiarity with regulatory guidelines and standards (FDA and Global; e.g., ISO 14155, ICH).
• Experience in medical device or pharmaceutical clinical trials.
• Familiarity with data visualization tools (Tableau, Spotfire, R Shiny, Python Dash).
• Benefits : We offer a comprehensive benefits package for full-time employees. This includes health, dental, and vision insurance, life, short-term and long-term disability insurance, 401(k), paid time off, and more.
• We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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