Technical Officer – SAS Programming (Clinical Trials)
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Req ID: 1590
Date: May 11, 2026
CTC Range: ₹3,50,000 – ₹7,00,000 per annum
Company Overview
Lambda Therapeutic Research Ltd. is a global Clinical Research Organization (CRO) headquartered in India with operations across Europe and the United States. The company provides full-spectrum clinical trial services for pharmaceutical and generic drug development, supported by global clinical research facilities and experienced scientific teams.
Role Summary
The SAS Programmer (Late Phase – Technical Officer) is responsible for:
Clinical trial statistical programming for early and late-phase studies
Development of analysis datasets and statistical outputs
Supporting CDISC-based clinical data standards
Ensuring high-quality programming deliverables for regulatory and clinical reporting
Key Responsibilities
1. SAS Programming & Statistical Outputs
Develop Tables, Listings, and Figures (TLFs) using SAS
Support programming for early and late-phase clinical trials
Generate and validate clinical trial outputs
2. Dataset Development (CDISC Standards)
Create and manage:
SDTM datasets
ADaM datasets
Ensure compliance with CDISC standards
Support submission-ready datasets
3. Quality Control (QC)
Perform programming-based QC of SAS deliverables
Validate datasets and TLF outputs
Ensure accuracy, consistency, and regulatory compliance
4. Regulatory Documentation Support
Assist in creation of:
define.xml
CSR-related documentation (e.g., CSR datasets support)
aCRF (annotated Case Report Forms)
ADRG / SDRG documents
5. Study Design & SAP Support
Provide inputs for Statistical Analysis Plans (SAPs)
Review programming notes and mock shells
Support statistical planning through technical insights
6. Team Support & Coordination
Support senior programmers and biostatistics team
Participate in training and knowledge sharing
Assist in quality improvement initiatives
7. Compliance & Standards
Follow SOPs and clinical research guidelines
Ensure compliance with CDISC and regulatory submission requirements
Maintain documentation for audit readiness
Required Skills & Experience
Technical Skills
Minimum 1 year SAS programming experience in clinical research
Strong knowledge of:
Base SAS / Advanced SAS
SDTM & ADaM datasets
TLF generation
Understanding of CDISC standards
Educational Qualifications
Postgraduate degree in:
Science
Statistics
Pharmacy
SAS Base or Advanced Certification (mandatory)
Experience Requirement
1–3+ years in pharma/CRO SAS programming environment (preferred 3+ years overall exposure)
Preferred Competencies
Experience in late-phase clinical trials
Exposure to regulatory submissions
Good analytical and problem-solving skills
Ability to work in team-oriented CRO environment
Attention to detail in data validation and QC
Work Environment
Based in Ahmedabad, India
Clinical research and CRO programming environment
Collaboration with global pharmaceutical clients
Structured, process-driven regulatory workflows
Role Impact
Supports accurate clinical trial reporting
Enables regulatory submission-ready datasets
Ensures compliance with global CDISC standards
Contributes to successful drug development programs
Career Path
This role can lead to:
Senior SAS Programmer
Statistical Programmer (SDTM/ADaM specialist)
Biostatistics Programming Lead
Clinical Data Standards Specialist
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