Posted:3 weeks ago|
Platform:
Work from Office
Full Time
Job Title: Senior SAS Programmer Experience: 510 Years Location: Bangalore (BLR) Notice Period: 0–30 Days Employment Type: Full-time Job Summary: We are looking for a Senior SAS Programmer with strong experience in clinical trial data programming. The ideal candidate will have expertise in SAS, SQL, and statistical reporting to support data analysis for clinical research studies. You will work closely with biostatisticians, data managers, and clinical teams to ensure the accuracy and quality of clinical trial outputs. Key Responsibilities: Develop and validate SAS programs to generate statistical summary tables, listings, and graphs (TLGs) . Create derived datasets for analysis using complex data manipulation techniques (e.g., LOCF, adverse events merging). Perform quality control (QC) on programs, datasets, and outputs. Support the development of Statistical Analysis Plans (SAPs) . Review CRFs and clinical databases for programming consistency. Compile and present clinical data reports and progress updates to the Biostatistics team. Import and process external data into analysis-ready formats. Participate in cross-functional team discussions to support clinical trial programming needs. Maintain detailed program documentation and contribute to internal QC and compliance processes. Required Skills: SAS (Base, Macros) SQL TLG generation Data derivation & transformation Clinical data standards LOCF, adverse event processing Experience with EDC systems Strong understanding of clinical trial design & data analysis Preferred: Experience in medical device clinical trials Familiarity with regulatory submission standards (e.g., CDISC, ADaM, SDTM) Soft Skills: Strong analytical and problem-solving skills Excellent communication and documentation abilities Attention to detail and quality focus Ability to manage timelines across multiple studies
Bean Hr Consulting
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