Programmer (SAS - Clinical Trials)

2 weeks ago


Nottingham, United Kingdom Worldwide Clinical Trials Full time

It is built by those who take pioneering, creative approaches and implement them with quality and excellence.


We are Worldwide Clinical Trials, and we are a global team of almost 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.


What Global Programming does at Worldwide


The Worldwide team is an experienced and diverse group of Programmers who collaborate together as one, both via regularly scheduled group meetings to discuss issues, and impromptu one-on-one discussions between colleagues to discuss a particular topic.


As a Statistical Programmer 2 on a project - you will be working with statisticians, sponsors, the wider study team and your own team of programmers, ensuring the data and output delivered for a study meets industry, regulatory submission and quality standards. As a Statistical Programmer 2 at Worldwide, you will develop SAS programs for the statistical reporting of clinical study data, ensuring that all processing is accurate and in compliance with department systems. Depending on experience you will also have the opportunity to be a Lead on some of your studies.


Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures and listings (TFL).
Perform review of the clinical database specification, data transfer agreement/specification, programming related parts of Statistical Analysis plan including TFL shells for medium complexity studies. Develop and review specification for SDTM datasets and ADaM datasets for safety data, TFL shells and other specifications, e.g. patient profiles, OPS reports.
Serve as a programming project lead on medium complexity studies (e.g. multy-part phase I study, parallel group phase II/III study with multiple endpoints) to distribute and oversee tasks for the programming team, communicate with internal and external clients, plan and execute delivery, and manage resources and competing project priorities with line manager or mentor support. Ensure budget and scope of project work remain aligned.
Contribute to department process improvement including creating and testing standard SAS Macros, maintaining the required validation documentation. Act as a mentor for junior department members.

Must be computer literate and numerate with a willingness to adapt to various computer systems.
Statistical programming skills and knowledge across a broad range of applications together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
The jobholder has worked as a Statistical Programmer within clinical trials with knowledge in SAS/Macro, Proc Report and ODS. Good working knowledge in SAS/Graph, Proc SQL.

Why Worldwide


At Worldwide, we balance fun with the serious business of changing lives. Interested in hearing more about Worldwide or our roles?



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