Vueverse has announced career opportunities for experienced Statistical Programmers, Clinical SAS Programmers and Biostatisticians across India. Professionals with 1–15+ years of experience in clinical programming, CDISC standards, statistical analysis and clinical trial data may explore these current and upcoming openings.
The hiring initiative connects clinical biometrics professionals with leading contract research organizations (CROs), pharmaceutical companies and biotechnology organizations. Candidates at junior, mid-level, senior and leadership stages may be considered depending on the requirements of each client opportunity.
Job Overview
| Particular | Details |
|---|---|
| Company | Vueverse |
| Roles | Statistical Programmer; Clinical SAS Programmer; Biostatistician |
| Location | Across India |
| Job type | Not specified; may vary by client opportunity |
| Experience | 1–15+ years |
| Qualification | Relevant degree not specified; suitable backgrounds are explained below |
| Salary estimate | Approximately ₹4.5 lakh–₹40 lakh per year, depending on role and experience |
| Posted date | July 27, 2026 |
| Last date | Not specified |
Roles and Responsibilities
The original announcement lists key areas of experience rather than detailed duties. Based on those requirements, shortlisted professionals may handle the following responsibilities, depending on the assigned role and client.
1. Statistical Programmer
- Develop and validate SAS programs for clinical trial analysis.
- Create efficacy and safety tables, listings and figures (TLFs).
- Work with ADaM datasets and applicable CDISC standards.
- Implement statistical analysis plan requirements in programming outputs.
- Perform quality control and validation of datasets, programs and outputs.
- Collaborate with biostatistics, clinical data management and study teams.
2. Clinical SAS Programmer
- Program and validate SDTM and ADaM datasets using SAS.
- Generate tables, listings and figures for clinical study reporting.
- Apply CDISC implementation standards and sponsor specifications.
- Conduct independent quality control of datasets and statistical outputs.
- Resolve programming issues and maintain clear documentation.
- Support regulatory submission deliverables where required.
3. Biostatistician
- Contribute to clinical study design and protocol development.
- Prepare or review statistical analysis plans.
- Perform sample-size estimation and statistical analyses.
- Analyze clinical trial data using SAS and/or R.
- Interpret findings and support clinical study reports.
- Work with programmers, clinicians, data managers and cross-functional stakeholders.
Qualifications and Who Can Apply
Vueverse has not stated mandatory educational qualifications in the source announcement. Based on the job responsibilities, candidates with the following backgrounds may be suitable:
- M.Sc. or Ph.D. in Statistics, Biostatistics, Applied Statistics or Mathematics
- M.Sc. in Bioinformatics, Data Science or a closely related quantitative discipline
- B.Pharm, M.Pharm, Pharm.D or a life-sciences degree combined with relevant Clinical SAS, CDISC or statistical programming experience
- B.E., B.Tech, MCA or another technical degree with proven clinical SAS programming and clinical-trial domain experience
Applicants should have at least one year of directly relevant experience. The exact degree, experience band and seniority will depend on the specific CRO, pharmaceutical or biotechnology client requirement. A relevant certification may strengthen an application but should not be treated as a substitute for hands-on experience unless Vueverse confirms otherwise.
Skills Required
Technical Skills
- SAS programming
- SDTM and ADaM dataset development
- Tables, listings and figures programming
- SAS and/or R for statistical analysis
- Program validation and quality control
- Sample-size estimation
- Statistical analysis plan implementation
Domain Skills
- CDISC standards
- Clinical trial data analysis
- Safety and efficacy reporting
- Study design and protocol development
- Clinical biometrics
- Regulatory submission support
Soft Skills
- Strong analytical and problem-solving ability
- Attention to detail and data quality
- Clear technical documentation
- Cross-functional communication
- Time and priority management
Experience Requirements
These Vueverse statistical programming and biostatistics opportunities cover a broad range of experience levels:
- Junior professionals: 1–3 years
- Mid-level professionals: 4–7 years
- Senior professionals: 8–12 years
- Lead or leadership professionals: 13–15+ years
Role availability at each level may depend on current and upcoming client mandates.
Estimated Salary
Vueverse has not disclosed compensation. The following broad estimates are indicative only and may vary by employer, location, technical expertise and seniority:
| Role | Estimated annual salary |
| Statistical Programmer | ₹5 lakh–₹35 lakh |
| Clinical SAS Programmer | ₹4.5 lakh–₹32 lakh |
| Biostatistician | ₹6 lakh–₹40 lakh |
Benefits
Benefits were not clearly specified in the job description. Compensation, work arrangement, insurance, leave, bonuses and other benefits may vary according to the hiring CRO, pharmaceutical company or biotechnology organization.
How to Apply
Application Link For Statistical Programmer
Application Link For Clinical SAS Programmer
Application Link For Biostatistician