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.Skills Required
Sas, Proc Sql, Sas Macros