
Medtek.AI is a data science-driven company based in India, specializing in accelerating drug development and healthcare solutions for the pharmaceutical and biotechnology industries. They offer a comprehensive suite of services including Generative AI content development, Data Science Consulting, Cloud (AWS) setup and support, Server setup and support, and GCP compliance and system validation. The company leverages its team of senior statisticians, data scientists, and programming experts to provide end-to-end support in biostatistics, programming, data management, visualization, and regulatory reporting. Medtek.AI aims to minimize costs and maximize productive outcomes for its clients by providing flexible, innovative, and reliable services. They support clients across North America, Japan, and the EU, focusing on building long-term relationships and delivering customer-centered services with cost-saving innovations.

Medtek.AI is a data science-driven company based in India, specializing in accelerating drug development and healthcare solutions for the pharmaceutical and biotechnology industries. They offer a comprehensive suite of services including Generative AI content development, Data Science Consulting, Cloud (AWS) setup and support, Server setup and support, and GCP compliance and system validation. The company leverages its team of senior statisticians, data scientists, and programming experts to provide end-to-end support in biostatistics, programming, data management, visualization, and regulatory reporting. Medtek.AI aims to minimize costs and maximize productive outcomes for its clients by providing flexible, innovative, and reliable services. They support clients across North America, Japan, and the EU, focusing on building long-term relationships and delivering customer-centered services with cost-saving innovations.
Key Responsiblities
Strong SAS data manipulation, analysis and reporting skills- with strong output programming experience
Strong 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