Senior Statistical Programmer - UK (Remote/Office/Hybrid)

JR United Kingdom; Shrewsbury; Hybrid; GBP 45,000 - 70,000; Full time

Job summary

A leading consultancy offers an exciting opportunity for a Senior Statistical Programmer to join their team in the UK. This role involves providing programming support across various projects, ensuring compliance with standards, and mentoring junior members in a supportive working environment. Suitable candidates will have a numerical background and a track record in programming.

Benefits

Supportive and friendly working environment

Opportunities for management and personal development

Innovative management practices

Qualifications

• At least 4 years of relevant experience.
• Familiar with data checks and statistical analysis methods.
• Experience in leading study team meetings.

Responsibilities

• Perform consistency review of clinical trial documents.
• Program and QC datasets and TFLs in SAS.
• Lead study team meetings and present updates.

Skills

SAS

Statistical Techniques

Data Validation

Project Management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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Senior Statistical Programmer - UK (Remote/Office/Hybrid), Shrewsbury

Client: Veramed

Location: Shrewsbury, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 3

Posted: 06.06.2025

Expiry Date: 21.07.2025

Job Description:

Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working environment supporting career growth.

We have an exciting opportunity for Senior Statistical Programmers to join us on a permanent basis in the UK. We offer home and/or office working, training, support, and a competitive package.

The role involves providing programming support across various projects, clients, and therapeutic areas.

Key Responsibilities

Technical

• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review study TFL shells and dataset standards
• Perform data checks and exploration (e.g., frequencies, histograms)
• Program and QC datasets and TFLs in SAS following specifications
• Complete and review CDISC Validation reports
• Ensure standards are applied and adhered to
• Familiar with simple statistical techniques (t-test, ANOVA, regression, survival analysis)
• Review project management documents
• Maintain audit-ready study master files and related documents

General

• Lead study team meetings and present updates
• Share knowledge within the team and with colleagues
• Ensure compliance with applicable regulations and policies
• Build collaborative relationships with team members
• Develop innovative ideas and contribute to process improvements
• Mentor junior team members
• Contribute to training materials and internal initiatives

Qualifications:

• BSc, MSc, or PhD in a numerical discipline or relevant industry experience
• At least 4 years of relevant experience

What To Expect

• A supportive and friendly working environment
• Management policies that support your development
• Unique CRO environment with innovative management
• Opportunities to own your role and develop skills