Vueverse, a growing clinical research organization (CRO), is hiring a Statistical Programmer – Junior Level for its Bengaluru, Karnataka location. This full-time, on-site role is ideal for candidates with 1–2 years of experience in SAS statistical programming who are looking to build a strong career in clinical trials, CDISC compliance, and regulatory submissions.
The position offers hands-on exposure to SDTM, ADaM, TLFs, and clinical study reporting, working closely with biostatisticians and cross-functional clinical teams in a regulated CRO environment.
Key Responsibilities
- Develop, maintain, and validate SAS programs for clinical trial data analysis
- Create SDTM and ADaM datasets in compliance with CDISC standards
- Generate high-quality Tables, Listings, and Figures (TLFs)
- Perform QC and independent validation of datasets and outputs
- Support interim, final analyses, and Clinical Study Reports (CSRs)
- Ensure adherence to SOPs, GxP, and regulatory guidelines
- Maintain complete programming documentation and version control
- Collaborate with biostatistics, data management, and clinical teams
Required Qualifications & Skills
- 1–2 years of experience in statistical programming within a CRO or clinical research environment
- Strong proficiency in SAS (Base SAS, SAS Macros)
- Hands-on knowledge of CDISC standards – SDTM and ADaM
- Understanding of the clinical trial lifecycle
- Experience working in a regulated, deadline-driven environment
- Strong analytical, problem-solving, and communication skills
Salary & Benefits
- Salary Range: ₹4,00,000 – ₹7,00,000 per annum (INR)
- Opportunity to work on global clinical trials
- Exposure to regulatory submissions and industry-standard datasets
- Career growth in biostatistics and statistical programming
- Collaborative and learning-driven CRO work culture
Job Location
📍 Bengaluru, Karnataka, India
🕒 Full-time | On-site
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How to Apply
