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Permanent

Tools & Standards Specialist/Principal Statistical Programmer (FSP)

London
money-bag Negotiable
Posted Today

Overview

Sponsor-dedicated: Working fully embedded within 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 new program.Position Overview:

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 SAS as well as experience participating and leading in standardization and automation. We are looking for a highly experienced 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.Responsibilities

Participate in developing and maintaining

our client''s

Statistical Computing Environment (SCE) . This may include standard setups but also customized

Visual Studio Code extensionsDeveloping and maintaining

solutions in SAS , potentially also expanding into

R

or

Python .Contributing to

workflow automation in compliance with CDISC standards

for ADaM, SDTM datasets and the production of tables, listings and figures (TLF).Designing and implementing

applications and other tools for internal use

in support of improved and scalable processes.Create

proof-of-concept models

to demonstrate innovative new ideas.Work with cross-functional teams; identify opportunities to drive automation and efficient operations.Qualifications

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:At least 8 years of SAS programming

experience in a drug development setting.Having worked on large and complex projects

that involve collaboration across different functions.Strong experience with Statistical Computing platforms.High sense of accountability while working indepently , with minimal need for supervision.Good Team Player and Driver capabilitiesDeep knowledge of

CDISC ADaM and SDTM

standards.Experience producing

Tables, Listings, and Figures (TLFs) .Experience and skill in

application development and automation .Experience with

Git

for collaboration and version control.Experience leading

proof-of-concept applications

and interacting with various stakeholders.A flexible and creative mindset with strong problem-solving skills.Being proactive and having the desire to

improve upon the existing processes .Preferred Qualifications (nice to have)

Familiarity with other programming languages such as

Python .Familiarity with

Domino Data ..... full job details .....

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