SAS Clinical Programmer / Statistical Programmer

Tata Consultancy Services; Gandhinagar; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Tata Consultancy Services is seeking a SAS Clinical Programmer to join our clinical data management team in a pharma/ CRO environment. You will develop SDTM datasets, create Define.xml, and build SAS macros to streamline programming tasks.

Ideal candidates have 3–12+ years of hands-on SAS programming experience in clinical research, with strong SDTM knowledge and CDISC standards familiarity. Collaboration with clients and delivering high-quality deliverables are key aspects of the role.

Qualifications

• Pharma/Clinical Research experience mandatory.
• Strong hands-on SAS Programming & SDTM experience.
• Knowledge of CDISC standards and clinical trials.
• Experience in SDTM mapping and validation.

Responsibilities

• Develop SDTM datasets and mapping specifications.
• Perform Define.xml generation and compliance validation.
• Develop SAS macros, utilities, and automation programs.
• Review programming deliverables and support study execution.
• Collaborate with clients and contribute to project delivery.

Skills

SAS Programming

SDTM

CDISC Standards

Clinical Trial Data Management

Tools

SAS

Job description

We are hiring for a SAS Clinical Programmer / Statistical Programmer

Experience: 3 to12+ Years

Domain: Pharma / Clinical Research (Mandatory)

We are hiring experienced SAS Clinical Programmers with expertise in SAS Programming, SDTM, CDISC Standards, and Clinical Trial Data Management.

Responsibilities

• Develop SDTM datasets and mapping specifications.
• Perform Define.xml generation and compliance validation.
• Develop SAS macros, utilities, and automation programs.
• Review programming deliverables and support study execution.
• Collaborate with clients and contribute to project delivery.

Mandatory Requirements

• Pharma/Clinical Research experience mandatory.
• Strong hands-on experience in SAS Programming & SDTM.
• Knowledge of CDISC standards and clinical trials.
• Experience in SDTM mapping and validation.