About the Role
We are seeking an experienced Senior SAS Programmer to join our team and contribute to the success of clinical research projects. In this role, you will develop, validate, and execute SAS programs for clinical trial data analysis and reporting. Key responsibilities include creating and validating datasets (SDTM and ADaM) and delivering TLFs (Tables, Listings, and Figures) in compliance with regulatory standards. Your technical expertise and commitment to high-quality deliverables will play a vital role in advancing our mission.
Requirements
Experience: Minimum 5 years of SAS programming in a clinical research environment.
Technical Skills: Proficiency in CDISC standards (SDTM, ADaM) and experience with TLF creation.
Education: Degree in statistics, computer science, life sciences, or a related field.
Knowledge: Familiarity with regulatory submission requirements (e.g., FDA, EMA).
Soft Skills: Strong problem-solving abilities, attention to detail, and teamwork.
Qualification
Experience with regulatory submissions.
Full SAS programming proficiency
Advanced statistical programming knowledge.
Familiarity with tools like Pinnacle 21 and R.
Responsibilities
Develop and validate SAS programs for clinical trial data analysis.
Ensure compliance with CDISC standards, including SDTM and ADaM.
Produce TLFs for regulatory submissions and internal review.
Collaborate with biostatisticians, data managers, and other programmers.
Troubleshoot and optimize workflows to meet project deadlines.