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Senior Software Developer

1 month ago

Stevenage, Hertfordshire, United Kingdom GSK Full time
Job Description

Job Title: Principal Programmer

GSK Clinical Programming brings together 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, and Respiratory. We 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 possess strong technical and excellent communication skills. They identify programming and/or process-related gaps and problems, providing logical and analytical solutions. They are experts in their TA-specific domains, providing technical and domain-area-specific training to colleagues. They represent the programming team, study, or therapeutic area cross-functionally, acting as the key point of contact for programming-related queries.

Principal Programmers act as the Study Lead Programmer, making significant contributions 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. They participate in or lead capabilities and non-project initiatives, present at internal forums, and learn new programming languages.

  • 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).

Key Qualifications

We are looking for professionals with the following required skills:

  • 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

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.
  • 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.
  • Expertise in representing programming function in cross-functional meetings, initiatives, and working groups.
  • Strong interest in or experience contributing to external organizations.