Clinical SAS Programmer

Position: Clinical SAS Programmer

Experience: 3+ 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. - Valuable 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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