PHARMAFull-time
Technical Officer – SAS Programming – CT
AHMEDABAD (IN)ONSITEPOSTED: 8/6/2026
PHARMAFull-time
HIRING ORGANIZATIONLAMBDA THERAPEUTIC RESEARCH LTD.Technology
ROLE DEFINITION & RESPONSIBILITIES
Selected candidates will be responsible for
Develop SAS programs for clinical trial Tables, Listings, and Figures (TLFs).
Perform programming quality control (QC) for datasets and TLF outputs.
Generate SDTM and ADaM datasets following CDISC standards.
Prepare CDISC documentation including: Define.xml, aCRF, ADRG, CSDRG.
Support Statistical Analysis Plan (SAP) development with programming inputs.
Create mock shells and programming specifications.
Participate in programming process improvements.
Assist in team knowledge sharing and quality initiatives.
Ensure timely and accurate delivery of statistical programming deliverables.
REQUIRED VERIFIED SKILLS
SAS Programming
CDISC Standards
SDTM
ADaM
TLF Generation
COMPENSATION & REWARDS
₹3.5L - 7.0L per annum
The salary range of ₹3.5 LPA to ₹7.0 LPA aligns well with market standards for clinical SAS programmers with 3+ years of experience in CROs.
ORGANIZATION CONTEXT & CULTURE
Lambda Therapeutic Research Ltd. is actively hiring for this position.
INDUSTRY: Technology
EXPECTED CAREER ROADMAP
Joining Lambda Therapeutic Research offers opportunities to work on international clinical trials and CDISC-compliant regulatory submissions, accelerating career progression within Biostatistics and Statistical Programming.
APPLICATION ADVISORY
Ensure your resume highlights expertise in CDISC standards (SDTM, ADaM), SAS certification (Base/Advanced), and hands-on experience with TLFs and regulatory submissions.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.