Why Choose Us ? We have talented professional staff experts in clinical research, medical writing, IT services, data science, and software development. Our professionals are experts in keeping your priorities and goals to follow updated business trends. Our expertise drives cost efficiency to our client. We are flexible, innovative, reliable, and passionate. Let's collaborate We are extremely honoured and grateful to have such talented people in our team. Their selfless efforts and dedication towards giving out our clients with the best of their capabilities made us a renowned and reputed incorporation today. We are a forward-looking organization and are motivated by the trust and confidence that our mutually beneficial relationship with our customers will take them and us to unattained heights of the universe.

SR. SAS PROGRAMMER

Key Responsibilities:

- Strong SAS data manipulation, analysis and reporting skills- with strong output programming experience
- Solid proficiency implementing the latest CDISC SDTM / ADaM standards.




- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
- Development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures)
- Develop and review SAS programs for data analysis, tables, figures, and listings, and ensure accuracy and consistency of data output

Qualifications:

- Bachelor’s or Master’s degree in a data science field, e.g., statistics, mathematics, computer science, bioinformatics,
- Minimum 4 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry.
- Strong expertise in SAS programming, and proficiency in other statistical software such as R and Python
- Onsite in Noida , Uttar Pradesh

Mail Your CV : [email protected]

📌 SR. SAS PROGRAMMER (India)
🏢 Medtek.AI
📍 India