Principal Clinical Programmer/Lead Programmer

TN United Kingdom; London; Hybrid; GBP 45,000 - 80,000

Job description

Social network you want to login/join with:

Principal Clinical Programmer/Lead Programmer, London

Client: GSK

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: d3972261b0ec

Job Views: 4

Posted: 30.03.2025

Expiry Date: 14.05.2025

Job Description:

Job description
Site Name: UK – London – New Oxford Street
Posted Date: Mar 27 2025

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

Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK

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:

Principal Clinical Programmer/Lead Programmer role at GSK reports into the associate director or research unit head. Principal 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 Clinical Programmer/Lead Programmer 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.

• Acts as a subject matter expert and works as a lead within own discipline to investigate new technology as directed
• Ensures the collection of programs/outputs and issues are adequately managed for programming activities to achieve business outcomes
• Applies learning from previous activities to result in quicker and more efficient completion of the current task
• Shares learnings with peers and contributes to internal technical discussions/forums
• Initiates new directions and novel strategies to achieve department goals
• 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
• Makes decisions on the implementation of programming requirements for low-risk topics of work and can propose solutions for higher risk activities
• Contributes to the development or improvement of departmental policies and working practices
• 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)
• Identifies and addresses issues with assigned activities and works to develop solutions with internal teams and/or outsourced partners
• Effectively presents at internal forums and / or external professional industry meetings
• Demonstrates effective communication to outsourced partners on project deliverables
• Works effectively and proactively in multi-disciplinary teams and a matrix environment through effective listening and active participation in challenging discussions
• Able to understand and clarify boundaries of responsibility within own role; allocates decision making authority and task responsibility to others as appropriate.

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
• 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:

• Solid understanding of the pharmaceutical regulatory and publishing processes (e.g., 21 CFR Part 11)
• Expertise in therapeutic area specific requirements – Oncology experience preferred
• 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: Thursday 17th of April 2025 (COB)

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.

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.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [emailprotected] or 0808 234 4391. The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/