Senior Statistical

Key Responsibilities:

• Lead and execute programming deliverables for complex programming projects or multiple moderate-complexity studies.
• Manage programming team deliverables to ensure project objectives are met on time and to the highest quality standards.
• Create and validate safety and efficacy analysis datasets in adherence with CDISC and client-specific standards.
• Generate high-quality safety and efficacy tables, listings, and figures.
• Develop study-specific or general macros and finalize programming specifications.
• Ensure adherence to programming specifications and documentation requirements.
• Plan and organize workload effectively to meet project-specific timelines.
• Communicate proactively with the biostatistics team and stakeholders to achieve study goals.
• Apply strong knowledge of statistical concepts using SAS programming.
• Adapt to changing project priorities while maintaining focus on delivery timelines.
• Learn and apply new techniques and technologies to enhance efficiency.

Qualifications:

• Minimum degree in Life Sciences, Pharmacy, Statistics, or Software Engineering with 6+ years of experience in SDTM, ADaM, and TLF programming.
• Proficiency in creating and validating safety and efficacy tables and datasets.
• Strong SAS programming skills, including SAS/Base, PROC SQL, SAS/Stat, SAS Macros, and SAS/Graph.
• Familiarity with data structures (e.g., CDISC SDTM, ADaM) and software development lifecycle.