Principal Programmer - Clinical Programming
Site Name: UK - Hertfordshire - Stevenage, UK - London - Brentford, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence
Posted Date: Oct 18 2019
GlaxoSmithKline is one of the world's foremost pharmaceutical and healthcare companies, with statisticians and programmers working in Research and Development with a global footprint spanning the UK, US, Canada and India. The Biostatistics division includes a Clinical Programming department, covering all phases of clinical drug development and commercialisation in a wide range of therapeutic areas. Programming's deliverables form the core of all regulatory submissions, health authority assessments, safety updates and publications (for peer review journals and scientific meetings).
In recognition of the developing sophistication and technical requirements of the role, Clinical Programming was formed as a standalone department distinct to Clinical Statistics. Programming asset teams are now stepping up to achieve the goal of being the Biostatistics' leaders of delivery and execution, in a way that optimises, expedites and delivers to the highest quality. In addition to the group's activities supporting GSK's pipeline of drugs, key accountabilities include developing and implementing strategies for programming resourcing using both internal and external resource; driving CDISC implementation for the reporting of clinical trials; and identifying and implementing IT solutions to offer further benefit and efficiency for the group's activities.
The Clinical Programming team at GSK has a strong focus on innovative ways of working and we are leading the way to implement these innovations and embracing an evolution for increased data science skills; this is already resulting in the introduction of new programming languages, technology and software. Some of these initiatives include the pathway for adoption of R and Python open source coding into day to day programming tasks, exploring machine learning to drive efficiencies for clinical reporting, developing desktop visualisation capabilities and we even have an annual challenge for Programmers who are rewarded for bringing new innovations into the department. But it's not just about the tech! We also encourage involvement in other initiatives too and we focus on your personal development path, building your project and leadership skills, your inter-departmental liaison and collaboration skills and we provide you with opportunities to get closer to the science and decision making.
Within the clinical programming team Senior Programmers and Principal Programmers support, guide, or make a major contribution to the planning and execution of multiple programming activities for GSK clinical trials. They are accountable for creating, verifying, and documenting analyses of clinical data while adhering to study protocols, analysis plans and GSK / industry standards.
• Act as a subject matter expert and work as a guide within own discipline to investigate new technology as directed.
• Provide technical contribution to complex tasks.
• Ensure the collection of programs/outputs and issues are adequately managed for programming activities to achieve business outcomes.
• Apply learning from previous activities to result in quicker and more efficient completion of the current task.
• Share learnings with peers and contribute to internal technical discussions/forums.
• Initiate new directions and novel strategies to achieve department goals.
During the course of your application you will be requested to complete voluntary information which will be used in monitoring the effectiveness of our equality and diversity policies. Your information will be treated as private and will not be used in any part of the selection process.
If you require a reasonable adjustment to the application / selection process to enable you to demonstrate your ability to perform the job requirements please contact (+44) 0808 234 4391. This will help us to understand any modifications we may need to make to support you throughout our selection process.
When applying for this role, please use the 'cover letter' of the on-line application to describe how you meet the aptitudes for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.
Thank you for your interest in this opportunity.
BSc or higher in mathematics, statistics, data science, computer science or related discipline.
• Recognized expertise in SAS programming and SAS macro code development. Understanding of other SAS products (e.g. SAS/GRAPH, SAS Output Delivery System).
• A thorough understanding of the end to end clinical trial process.
• A solid level of understanding of the pharmaceutical regulatory and publishing processes (e.g. 21 CFR Part 11).
• Demonstrated knowledge of and experience in the application of CDISC data and standards, primarily the creation and use of ADaM datasets.
Experience with non-SAS programming packages/languages, particularly R, Python.
Project management or relevant experience.
Knowledge of basic computer skills (MS Word, Excel, PowerPoint, Outlook).
At GSK, our mission is to improve the quality of human life by enabling people to do more, feel better and live longer. Our three world renowned businesses research and deliver innovative medicines, vaccines and consumer healthcare products. We need a talented and motivated workforce to deliver against our strategy. To achieve this, we strive to attract the best people and to create an environment that empowers and inspires.
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