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If you’re looking to build a career in clinical data science and statistical programming, this Statistical Programmer job in Ahmedabad at Veeda Clinical Research (Veeda CR) offers a strong entry point. With demand rising for professionals skilled in SAS programming, CDISC standards, and clinical trial data, this role aligns well with candidates having 1โ3 years of experience in the pharmaceutical and CRO domain.
๐ Job Overview
- Role: Statistical Programmer
- Company: Veeda Clinical Research (Veeda CR)
- Location: Ahmedabad, India
- Experience: 1โ3 years
- Salary: โน4,00,000 โ โน6,50,000 per annum
- Job Type: Full-time, Permanent
- Openings: 1
- Posted On: April 9, 2026
๐ Key Responsibilities
As a Statistical Programmer, you will be responsible for handling clinical trial datasets and ensuring regulatory compliance using industry standards like CDISC:
- Prepare Annotated Case Report Forms (aCRF) using Adobe Acrobat
- Develop SDTM and ADaM mapping specifications
- Create and maintain SAS programs for clinical data analysis
- Generate Define.xml and metadata using Pinnacle 21
- Build CDISC-compliant datasets (SDTM, ADaM)
- Run Pinnacle 21 validation checks and resolve issues
- Prepare cSDRG and ADRG reports per FDA guidelines
- Perform data validation and edit checks
- Provide timely QA responses and documentation support
- Utilize SAS Macros for automation and efficiency
๐ Qualifications & Skills Required
Educational Background
- B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biostatistics, or related field
Technical Skills
- Strong knowledge of SAS programming
- Hands-on experience with CDISC standards (SDTM, ADaM)
- Familiarity with Pinnacle 21 Validator
- Understanding of clinical trial data workflows
- Experience in Define.xml and metadata generation
Soft Skills
- Analytical thinking and problem-solving
- Attention to detail in regulatory deliverables
- Good communication with cross-functional teams
๐ผ Why Choose This Role?
- Opportunity to work in a growing Clinical Research Organization (CRO)
- Exposure to global regulatory standards (FDA, CDISC)
- Hands-on experience with real-world clinical trial data
- Career progression in biostatistics and data science
- Competitive salary package for early-career professionals
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๐ฉ How to Apply
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