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A leading biostatistics consulting firm in Greater London is seeking a Tools and Standards Specialist to support a global pharmaceutical client. This role requires at least 8 years of experience in programming, particularly in R, and familiarity with CDISC standards. The candidate will be responsible for automating clinical data processes and implementing workflows. A team player with strong problem-solving skills is essential for this position, which offers opportunities for innovation and professional growth.
Working fully embedded within a tools and standards development team of one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Tools and Standards Specialist you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this program.
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Tools and Standards Specialist will have a background in Statistical Programming using R and (desirably) SAS as well as experience participating and leading in standardization and automation. We are looking for highly talented and technically skilled specialist who can convert their knowledge into tools that help make reporting of data from clinical trials and projects more efficient with high quality.
Participate in developing and maintaining solutions based on R and other languages/tools .
Implement and maintain workflows in compliance with CDISC standards , using R toolchains
Automate clinical (and statistical) data processes , with an aim to provide tools that are scalable for repeated use
Identify opportunities for automation in collaboration with cross-functional team.
Create proof-of-concept models to demonstrate innovative new ideas and drive towards production-ready solution.
Support documentation, sharing of knowledge, process improvement.
At least 8 years of programming experience in a drug development setting; strong with R, SAS is desirable.
Experience developing R Shiny web apps and validating R packages.
Strong understanding of CDISC standards for SDTM and ADaM and experience in development of tables, listings and figures.
High sense of accountability while working independently .
Good Team Player and Driver capabilities
A flexible and creative mindset with strong problem-solving skills . Strong cross-functional collaborator who is able to explain technical matters in lay language.
Being proactive and having the desire to improve upon the existing processes .
Familiarity with other programming languages such as Python .
Git knowledge
Familiarity with Domino Data Lab
Experience supporting customers and users, including giving training
Cytel Inc. is an Equal Employment / AffluentEmployer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.