Are you an experienced SAS Programmer looking to build your career in a leading Clinical Research Organization (CRO)? Lambda Therapeutic Research Ltd. is hiring Technical Officer โ SAS Programming (Clinical Trials) for its Biostatistics & Programming team in Ahmedabad, Gujarat.
This opportunity is ideal for professionals with expertise in SAS Programming, CDISC standards, SDTM, ADaM, TLF generation, and clinical trial data programming. Candidates with experience in pharmaceutical companies or CROs and strong programming skills can accelerate their careers with one of India’s leading global CROs.
Job Details
| Particular | Details |
|---|---|
| Job Title | Technical Officer โ SAS Programming โ CT |
| Company | Lambda Therapeutic Research Ltd. |
| Department | Biostatistics & Programming |
| Location | Ahmedabad, Gujarat |
| Employment Type | Full Time |
| Industry | Clinical Research / CRO |
| CTC Range | โน3.5 โ โน7.0 LPA |
About Lambda Therapeutic Research
Lambda Therapeutic Research Ltd. is a globally recognized Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations across India, Poland, the UK, and the USA, the company delivers comprehensive clinical trial solutions for pharmaceutical, biotechnology, and generic drug companies.
With more than two decades of experience and over 1,500 professionals worldwide, Lambda specializes in clinical research, bioequivalence studies, biostatistics, statistical programming, pharmacovigilance, and regulatory services.
Key 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 Qualifications
Candidates should possess:
- Postgraduate degree in:
- Pharmacy
- Statistics
- Life Sciences
- Science
- Mandatory SAS Base or SAS Advanced Certification
- Experience in SAS Programming within the pharmaceutical or CRO industry.
- Strong understanding of:
- Clinical Trial Programming
- CDISC Standards
- SDTM
- ADaM
- SAS Programming
- Statistical Programming
Experience Required
- 3+ years of SAS Programming experience in a pharmaceutical company or CRO.
- Experience working on clinical trial statistical programming projects.
- Prior exposure to regulatory submission datasets is preferred.
Preferred Skills
- SAS Base Programming
- SAS Advanced Programming
- Clinical Trial Data Analysis
- CDISC Implementation
- SDTM Programming
- ADaM Dataset Creation
- TLF Programming
- Define.xml Generation
- Statistical Analysis Plan (SAP)
- Clinical Data Standards
- Good Documentation Practices
- Quality Control Programming
Salary
Expected CTC: โน3.5 LPA โ โน7.0 LPA
Actual compensation may vary depending on experience, technical expertise, certifications, and interview performance.
Why Join Lambda Therapeutic Research?
- Work with a leading global Clinical Research Organization.
- Exposure to international clinical trials.
- Opportunity to work on CDISC-compliant regulatory submissions.
- Career growth in Biostatistics and Statistical Programming.
- Collaborative work environment with experienced programming teams.
- Learn advanced SAS programming practices for global studies.
How to Apply
