Clinical SAS Programmer – SAS & R Programming
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Job Description
Job Opening: Clinical SAS Programmer – SAS & R Programming
Experience: 3+ Years
Work Mode: Work From Home (WFH)
Location: Pan India
Notice Period: 30–60 Days
Job Description
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.
Mandatory Skills
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.
Key Responsibilities
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.
Candidate Requirements
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.
Work Arrangement: Permanent Work From Home | Pan India
Notice Period: 30–60 Days
Requirements
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.