SAS Clinical Programmer / Statistical Programmer

Tata Consultancy Services; Ahmedabad District; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Tata Consultancy Services in Ahmedabad is hiring a SAS Clinical Programmer / Statistical Programmer with 3 to 12+ years of Pharma/Clinical Research experience.

You will develop SDTM datasets, mapping specifications, Define.xml, SAS macros, utilities, and automation programs for trials while collaborating with client teams.

Candidates should have hands-on SAS programming, SDTM mapping, CDISC standards, and familiarity with regulatory requirements (FDA/ICH-GCP) to support study delivery.

Qualifications

• Pharma/Clinical Research experience mandatory
• Strong hands-on SAS Programming & SDTM
• 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

Base SAS

Advanced SAS

SAS Macros

SQL

CDISC Standards SDTM/ADaM/CDASH

SDTM Mapping

Define.xml

Clinical Trial Data Programming

Regulatory Standards

Tools

SAS

Job description

We are hiring for a SAS Clinical Programmer / Statistical Programmer

Experience: 3 to12+ Years

Domain: Pharma / Clinical Research

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

Key Skills

• Base SAS, Advanced SAS, SAS Macros, SQL
• CDISC Standards (SDTM, ADaM, CDASH)
• SDTM Mapping & Define.xml
• Clinical Trial Data Programming
• Controlled Terminology & TAUG
• FDA, ICH-GCP & Regulatory Standards

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