Principal / Senior Statistical Programmer

Company Description

Veramed is a customer-driven Clinical Research Organisation (CRO), providing high-quality biostatistics and programming services to the pharmaceutical and biotech industry. Founded in 2012, Veramed acts as an extension to its clients' teams, ensuring collaboration and efficient, quality-driven outcomes that go above and beyond industry standards. Headquartered in Twickenham, England, with offices in Manchester, Swansea, as well as Europe and the US, Veramed is B Corp Certified® with people, patients, and the environment at its heart. Our expert team focuses on delivering high-quality analysis and consultancy of Phase I-IV clinical trials across various therapeutic areas.

Role Description

This is a full-time on-site role for a Principal / Senior Statistical Programmer located in Bengaluru South. The Principal / Senior Statistical Programmer will be responsible for developing, testing, and validating statistical programs for clinical trials, working with clinical trial data, creating and maintaining statistical programming documentation, and ensuring compliance with regulatory requirements. The role involves close collaboration with statisticians, data managers, and other team members to deliver high-quality programming solutions.

Qualifications

• Proficiency in statistical programming languages such as SAS and R
• Experience in developing, testing, and validating statistical programs for clinical trials
• Understanding of clinical trial data and regulatory requirements
• Strong analytical and problem-solving skills
• Excellent written and verbal communication skills
• Ability to work effectively in a collaborative, team-oriented environment
• Advanced degree in Statistics, Biostatistics, Computer Science, or a related field
• Experience in the pharmaceutical or biotech industry is a plus

Skills Required

Sas, statistical programming, Regulatory Requirements