Principal Programmer GSK Clinical Programming brings together some of the most talented minds to engage in advanced data analytics, principles of data science, and developing new computational tools to support innovative research and develop novel therapies. We serve five key therapeutic areas: HIV, Immunology, Infections Disease, Oncology, Respiratory, and Vaccines, and offer unlimited growth opportunities and exciting career paths for a wide range of experience levels. Your Role at GSK The Principal Programmer role at GSK reports into the associate director or research unit head. Principle Programmers are expected to possess strong technical and excellent communication skills. They are able to identify programming and/or process related gaps and problems and provide logical and analytical solutions to address these. They are experts in their TA-specific domains and are able to provide technical and domain area specific training to their colleagues. They represent the programming team, their study, or therapeutic area cross-functionally and act as the key point of contact for programming related queries. They are expected to demonstrate strong technical and/or study lead programmer skills, engage in external organizations, and successfully work with global teams. Principal Programmers act as the study lead programmer and offer significant contributions towards 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 for themselves and their team. Principal programmers are expected to participate in or lead capabilities and non-project initiatives, present at internal forums, and learn new programming languages. They interact with non-programming team members and represent their study during and function in core study team meetings. Reads and understands specifications to implement them in code Ensures the collection of programs/outputs and issues are adequately managed for programming activities to achieve business outcomes Identifies gaps in current programming practices and provides possible resolution suggestions Effectively communicates technical and complex approaches to peers and non-technical colleagues Project manages or leads programming activities under supervision, to achieve technical or business outcomes within own discipline Contributes to department strategies and key initiatives through working groups and sub teams Anticipates problems within discipline, proactively uses own expertise and/or seeks input from others, to recommend solutions and influence appropriate change Uses technical expertise to provide innovative solutions to project related problems of colleagues and of other projects within the research unit Develops responses to audit/inspection questions and complete CAPAs within agreed timelines Demonstrates appropriate engagement with outsourced partners. Performs and documents oversight of outsourced activities including Quality Assurance (QA) Why you? Qualifications & Skills: We are looking for professionals with these required skills to achieve our goals: A BSc, BA or equivalent in Mathematics, Statistics, Computer Science, or related subject Statistical programming and some level of lead experience in clinical R&D is required. Advanced proficiency in one or more programming languages, such as R, Python, and/or SAS Experience with using other clinical data analysis and reporting tools, such as Spotfire, SAS Azure, or S-Plus Advanced macro development and debugging, and executing complex programming activities skills Knowledge of standard macro development process Strong expertise in CDISC standards and its application Strong knowledge of Good Practice (GxP), and International Council for Harmonization (ICH) requirements Preferred Qualifications & Skills: If you have the following characteristics, it would be a plus: MSc or PhD (or equivalent) in Mathematics, Statistics, Computer Science or related subject preferred Solid understanding of the pharmaceutical regulatory and publishing processes (e.g., 21 CFR Part 11) Advanced expertise in end-to-end clinical trial process and application of key clinical documents Experience with mentoring and supervising junior programmers on technical tools and concepts Experience with outsourcing of statistical programming work in the clinical trials setting (e.g., working with CROs, academic institutions, etc.) Expertise in representing programming function in cross-functional meetings, initiatives, and working group Strong interest in or experience contributing to external organizations (e.g., PHUSE, PharmaSUG, etc.) Closing Date for Applications: 25th November 2024 Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies 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. At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong tech-enabled capabilities that allow us to build a deeper understanding of the patient, human biology and disease mechanisms, and transform medical discovery. We are revolutionising the way we do R&D. We’re uniting science, technology and talent to get ahead of disease together. Find out more: Our approach to R&D. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class(US only). We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. 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