Clinical SAS Programmer

Position : Clinical SAS Programmer
Experience : 5+ Years
Location: Mumbai/Pune/Bangalore/Noida
Salary: Up to 35 LPA
Employment Type : Full time

Key Responsibilities :
Develop and validate SDTM, ADaM, and TFLs using Base SAS and SAS Macros.
Perform statistical programming activities in compliance with CDISC standards.
Create and maintain Tables, Listings, and Figures (TFLs) based on Statistical Analysis Plans (SAPs).
Review protocols, Annotated CRFs, and specifications to develop submission-ready datasets.
Perform QC and validation of SAS programs and datasets.
Support regulatory submissions for global clinical studies.
Collaborate with Biostatistics, Clinical Data Management, and cross-functional teams.

Required Skills :
Strong experience in Base SAS,



SAS Macros, and SQL.
Hands-on experience with SDTM, ADaM, CDISC, TFL Programming, and Define.xml.
Good understanding of FDA/ICH regulatory guidelines.
Experience working on Phase I–IV clinical studies.
Excellent analytical, problem-solving, and communication skills.

Preferred
Experience across therapeutic areas such as Oncology, Diabetes, Cardiovascular, or Immunology.
Exposure to Pinnacle 21 and submission support will be an added advantage.

Interested candidates can share their updated resume at: [email protected] & [email protected]

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