
Senior Sas Programmer
3 weeks ago
This role involves end-to-end SAS programming for analysis and reporting, with a focus on regulatory compliance, data standards, and high-quality deliverables.
The ideal candidate should have strong experience in efficacy analysis, SDTM and ADa M generation, and TLF programming.
Key Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data, including both safety and efficacy datasets (ISS/ISE), using SAS.
Generate and validate SDTM and ADa M datasets in accordance with CDISC standards.
Create and validate Tables, Listings, and Figures (TLFs) for study reports and regulatory submissions.
Develop complex ad-hoc reports from raw clinical data.
Apply a strong understanding of efficacy analyses and clinical endpoints.
Contribute to the preparation and review of submission documents and electronic Case Report Tabulations (e CRTs).
Perform production programming and quality control (QC/validation) to ensure accuracy and consistency.
Act as a team player, demonstrating commitment to quality and meeting project deadlines.
Stay adaptable and flexible to shifting priorities in a fast-paced clinical environment.
Required Qualifications: Bachelor's or Master's degree in Life Sciences, Statistics, Computer Science, or a related field.7+ years of hands-on experience in clinical trial programming using SAS.
Proficient in CDISC standards (SDTM, ADa M), including mapping and validation.
Strong working knowledge of Base SAS, SAS Macros, SAS/STAT, and SAS/GRAPH.
Experience in generating datasets and outputs for regulatory submissions (including ISS/ISE).
Familiarity with e CTD standards, including Define.xml and dataset documentation.
Excellent attention to detail and strong analytical problem-solving skills.
Why Join Us?Join a collaborative team environment where your expertise in clinical data programming directly contributes to advancing global healthcare.
We value precision, integrity, and innovation in every project we undertake.
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