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Develop, maintain, and validate clinical trial datasets using SAS and R while ensuring compliance with regulatory standards. Generate Tables, Listings, and Figures (TLFs) and perform quality checks to support clinical study reports.
We are looking for experienced Clinical SAS Programmers with hands-on expertise in Clinical SAS Programming and R Programming to support clinical trial data analysis, statistical programming, and regulatory submissions.
Clinical SAS Programming – Mandatory
R Programming – Mandatory
Minimum 3+ years of relevant experience in SAS Programming.
At least 1 year of hands-on experience in R Programming is mandatory.
Strong knowledge of SDTM and ADaM standards.
Experience in developing and validating clinical trial datasets.
Knowledge of Tables, Listings, and Figures (TLFs).
SAS macros, data manipulation, statistical programming, and quality control.
Relevant Clinical SAS Programming certification is required.
Develop, maintain, and validate clinical trial datasets using SAS and R.
Create and validate SDTM and ADaM datasets.
Generate Tables, Listings, and Figures (TLFs) for clinical study reports.
Perform programming validation, quality checks, and discrepancy resolution.
Ensure compliance with clinical research standards and regulatory requirements.
Maintain accurate programming documentation and collaborate with biostatistics and data management teams.
Minimum 3+ years of experience in Clinical SAS Programming.
Minimum 1 year of hands-on R Programming experience is mandatory.
Practical experience with SDTM, ADaM, and clinical trial data.
Relevant certification in Clinical SAS Programming.
Strong analytical, problem-solving, and communication skills.
Important: Candidates with SAS experience but without at least 1 year of R Programming experience are not eligible for this requirement.
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