Senior programmer Work, Jobs in Watlington, Oxf (with Salaries)

Senior Principal Programmer (UK)
UCB —Slough
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Senior Technical Designer - Medidata RAVE Certification required
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Databases
- Quality control
Sr. Clinical Data Manager (Netherlands, United Kingdom)
Allucent —Bracknell
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bachelor's degree
- Training & development
- Flexible schedule
- Referral programme
Quick apply
Clinical Data Manager - FSP (Homebased - UK)
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Quality control
- Work from home
14d
Senior Statistical Programmer - Sponsor Dedicated
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Quality control
- Organisational skills
Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated
Fortrea —Maidenhead
- Full-time
- English
- Quality control
- Organisational skills
Graduate Programmer
Rebellion —Oxford
- Full-time
- C++
- Bachelor's degree
- Free parking
- Relocation assistance
Quick apply
19h
Principal Statistical Programmer - Sponsor Dedicated, EMEA
Fortrea —Maidenhead
- Full-time
- English
- Mentoring
Lead Statistical Programmer - Sponsor Dedicated
Fortrea —Maidenhead
- Full-time
- English
- Mentoring
Principal Statistical Programmer
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Team management
- Travel
- In-person

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Senior Clinical Data Manager - sponsor dedicated - oncology
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Senior Principal Programmer (UK)

UCB -
Slough

Apply Now

Job details

Permanent

Qualifications

Stakeholder collaboration
Stakeholder liaison
Process improvement
Technical support
IT permissions management
Clinical trials
Multidisciplinary collaboration
Pharmaceutical industry setting experience

Full job description

Make your mark for patients

We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in any of our Brussels (Belgium), Monheim (Germany), Raleigh (USA), or Slough (UK) offices.

About the role

You will help clinical programming teams move to and work confidently within UCB’s modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs.

Who you’ll work with

You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.

What you’ll do

You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.

You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.

You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.

You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.

You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.

You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.

Interested? For this position you’ll need the following education, experience and skills:

You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.

You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.

You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.

You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.

You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.

You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Apply Now

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senior programmer jobs in watlington, oxf

Senior Principal Programmer (UK)

Senior Clinical Data Manager - sponsor dedicated - oncology

Senior Technical Designer - Medidata RAVE Certification required

Sr. Clinical Data Manager (Netherlands, United Kingdom)

Clinical Data Manager - FSP (Homebased - UK)

Senior Statistical Programmer - Sponsor Dedicated

Senior or Principal Statistical Programmer - ONCOLOGY - Sponsor dedicated

Graduate Programmer

Principal Statistical Programmer - Sponsor Dedicated, EMEA

Lead Statistical Programmer - Sponsor Dedicated

Principal Statistical Programmer

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