Technical Officer – SAS Programming (Clinical Trials) | Lambda Therapeutic Research Ltd.
Job Details
Job Title: Technical Officer – SAS Programming (CT)
Job Role: SAS Programmer (Late Phase Clinical Trials)
Company: Lambda Therapeutic Research Ltd.
Job ID (Req ID): 1590
Location: Ahmedabad, Gujarat, India
Department: Biostatistics & Programming
Reporting To: Manager – Biostatistics / Senior SAS Programmer
Job Type: Full-time
CTC Range: ₹3.5 – ₹7.0 LPA
Posted Date: 8 July 2026
About the Company
Lambda Therapeutic Research Ltd. is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With over 20 years of experience and 1,500+ employees worldwide, the company provides end-to-end clinical research services to pharmaceutical, biotechnology, and generic drug companies across India, Poland, the UK, and the USA.
Job Purpose
The Technical Officer – SAS Programming will be responsible for SAS programming in early and late-phase clinical trials, including clinical datasets, statistical outputs, CDISC standards, quality control, and programming support for regulatory submissions.
Key Responsibilities
Perform SAS programming for Tables, Listings, and Graphs (TLGs) for early and late-phase clinical trials.
Conduct programmatic quality control (QC) for SAS deliverables, including datasets and TLGs.
Generate SDTM and ADaM datasets for clinical trials.
Create CDISC documentation such as:
Define.xml
cSDRG
ADRG
Annotated CRF (aCRF)
Provide programming inputs for the Statistical Analysis Plan (SAP), programming processes, and mock shells.
Support team activities, including resource management, training, and quality improvement initiatives.
Ensure compliance with CDISC standards, regulatory guidelines, and SOPs.
Collaborate with Biostatistics and Clinical Data Management teams.
Required Qualifications
Postgraduate degree in Science, Statistics, or Pharmacy.
SAS Base or Advanced Certification (Mandatory).
Experience in SAS programming within the pharmaceutical or CRO industry.
Knowledge of SDTM, ADaM, CDISC standards, and clinical trial programming.
Experience Required
Minimum 1 year of experience as a SAS Programmer in the Clinical Research or Life Sciences domain.
Preferred: 3+ years of SAS programming experience in a pharmaceutical or CRO environment.
Preferred Skills
SAS Programming (Base SAS & Advanced SAS).
SDTM and ADaM dataset creation.
CDISC standards implementation.
Tables, Listings, and Graphs (TLGs).
Statistical Analysis Plan (SAP) support.
Define.xml, cSDRG, ADRG, and aCRF preparation.
Clinical trial data programming.
Quality Control (QC) of SAS outputs.
Clinical research and regulatory compliance.
Team collaboration and mentoring.
One-Line Experience
Candidates with 1–3+ years of SAS Programming experience in clinical trials, along with expertise in SDTM, ADaM, CDISC, and TLG generation within a CRO or pharmaceutical company, are preferred.
Salary Package
Official CTC: ₹3.5 – ₹7.0 LPA
Market Standard: ₹5.0 – ₹9.0 LPA (depending on SAS expertise, CDISC knowledge, and relevant clinical trial experience).
Why Join Lambda Therapeutic Research?
Opportunity to work with a globally recognized Clinical Research Organization (CRO).
Hands-on experience with global clinical trial programming projects.
Exposure to CDISC standards, regulatory submissions, and advanced SAS programming.
Collaborative work environment with opportunities for learning and career growth.
Competitive compensation and long-term career development in clinical data programming.
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