Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, youll be at the heart of our clients innovation. As a Principal Statistical Programmer, you will be dedicated to
Key Accountabilities: Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances of study
3 to 5 Years of experience is required Should have Good experience in R shiny Strong R and RShiny/web development knowledge with package and code repository knowledge or management experience Programming languages and syntax: R, RShiny, Python, JavaScript/CSS Clinical standard
ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and