Location: India (Remote/Hybrid)

Employment Type: Full-time

Veramed is looking for an experienced Statistical Programmer to support the delivery of high-quality programming outputs for clinical trials.

What You'll Bring:

• 4+ years of Statistical Programming experience

• Experience in SAS and R

• Hands-on experience with SDTM , ADAM , TLFs

• Hands-on experience with both Safety and Efficacy analysis

Technical:

- Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
- Author and review simple and complex study TFL shells
- Author and review simple and complex dataset standards
- Perform data checks and data exploration (e.g. using frequencies, histograms)
- Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice
- Complete and review CDISC Validation tool reports
- Ensure the appropriate standards are being applied and adhered to
- Familiarization with straightforward statistical techniques (e.g. t-test, ANOVA, regression,



standard survival)
- Review of project management related documents
- Maintain study master file documents and any other documents that are required to be audit ready

Veramed is a B Corp accredited company which means that we use the power of business to build a more inclusive and sustainable economy meeting the highest verified standards of social and environmental performance, transparency, and accountability.

As an organization that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.

📌 Senior Statistical Programmer (India)
🏢 Veramed
📍 India