Principal Programmer

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

We’re uniting science, technology, and talent to get ahead of disease together.

Find out more:

Our approach to R&DJob Purpose We are seeking a Principal Programmer to join our Clinical Programming team, contributing to pipeline delivery across complex and pivotal studies. This role operates within an agile, squad-based environment, where you will lead study delivery, collaborate with cross-functional teams, and act as a technical mentor to ensure high-quality and timely outputs. Working closely with stakeholders across clinical, statistical, and operational functions, you will play a key role in bridging scientific requirements with technical solutions, supporting the successful execution of clinical development programmes within a global setting.

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.

We embrace modern work practices; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Key responsibilities include:

Independently lead programming activities for one or more studies, ensuring development, maintenance, and validation of complex analysis packages

Foster quality assurance by ensuring programming activities adhere to standards such as Good Programming Practices and CDISC standards.

Mentor junior programmers by providing guidance and support in technical programming tasks and industry best practices

Lead programming support for regulatory interactions (e.g., EMA, FDA)
Identify gaps and inefficiencies and recommend and implement innovative solutions aligned with standards and best practices

Establish and uphold governance frameworks, identify risks early and devise mitigation plans, ensuring timely escalation

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:5+ years of programming experience within the pharmaceutical, biotechnology, healthcare, or other regulated industry.

Experience programming in one or more languages such as SAS, R, Python, or a comparable programming language.

Experience supporting clinical trials, clinical development programs, or analysis of clinical research data.

Experience developing, validating, and maintaining custom programs, analyses, tables, figures, or listings.

Experience applying programming standards, quality control procedures, and regulatory requirements within a regulated environment.

Expertise in Oncology therapeutic area specific requirements like RECIST
1.1.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

Experience collaborating with cross-functional stakeholders to deliver programming or data analysis solutions.

Experience guiding others in the use of Artificial Intelligence/Machine Learning (AI/ML) tools or applying these tools to improve efficiency

Experience contributing to internal technical discussions, forums, or external technical organizations

Experience…