Statistical Programmer 2

4 weeks ago

Nottingham, United Kingdom Worldwide Clinical Trials Full time

**Requisition Number**
**6556**

**Employment Type***:
**Regular**

**Who we are**

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. 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.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

**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.

**What you will do**
- 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.

**What you will bring to the role**
- Must be computer literate and numerate with a willingness to adapt to various computer systems.
- It is essential that the job holder to possess strong analytical skills and attentiveness to detail.

**Your experience**
- Educated to degree level or equivalent.
- 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. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

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