Technical Officer – SAS Programming (Clinical Trials)
Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, Gujarat
Req ID: 1590
Employment Type: Full-Time
Department: Biostatistics & Programming
Reporting To: Manager Biostatistics / Sr. SAS Programmer
CTC Offered: ₹3.5 – ₹7 LPA
About the Role
Lambda Therapeutic Research is looking for a Technical Officer – SAS Programming to support programming activities for clinical trials. The role involves generating clinical datasets, developing Tables, Listings & Graphs (TLGs), performing quality checks, supporting CDISC deliverables, and contributing to statistical programming activities for clinical studies.
Key Responsibilities
SAS Programming
Develop SAS programs for clinical trial data analysis.
Generate:
Tables
Listings
Graphs (TLGs)
Statistical Outputs
Support programming activities for clinical studies.
Clinical Dataset Development
Create and validate:
SDTM Datasets
ADaM Datasets
Ensure compliance with CDISC standards.
Support dataset submission readiness.
Quality Control & Validation
Perform programmatic QC of:
Datasets
TLGs
Statistical Outputs
Identify and resolve programming discrepancies.
Ensure accuracy and quality of deliverables.
Regulatory Submission Support
Prepare CDISC submission documentation including:
Define.xml
SDRG (Study Data Reviewer’s Guide)
ADRG (Analysis Data Reviewer’s Guide)
Annotated CRF (aCRF)
Support regulatory submission activities.
Statistical Programming Support
Provide programming inputs for:
Statistical Analysis Plans (SAP)
Programming Specifications
Mock Shell Development
Collaborate with Biostatistics and Clinical teams.
Team & Process Support
Contribute to process improvement initiatives.
Support training and knowledge-sharing activities.
Assist in maintaining programming quality standards.
Required Qualifications
Education:
Postgraduate Degree in:
Pharmacy
Statistics
Life Sciences
Related Scientific Discipline
Certification:
SAS Base Certification (Mandatory)
SAS Advanced Certification (Preferred)
Required Experience
Minimum 1 year of Clinical SAS Programming experience.
Experience in Pharma, CRO, or Clinical Research industry.
Exposure to clinical trial datasets and reporting.
JD mentions exposure up to 3+ years in SAS Programming preferred.
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