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

JR United Kingdom; Altrincham; Remote; GBP 45,000 - 75,000; Full time

Job summary

An established industry player is seeking a Senior Statistical Programmer to join their dynamic team in the UK. This role offers the flexibility of remote, hybrid, or office work, along with a supportive environment that fosters professional growth. You will engage in programming support for clinical trials, ensuring compliance with industry standards while leading collaborative efforts across teams. With a focus on mentorship and knowledge sharing, this position is perfect for those looking to make a meaningful impact in their field. If you are passionate about statistics and programming, this is an exciting opportunity to advance your career.

Benefits

Training Opportunities

Career Support

Flexible Working Hours

Unique Company Culture

Qualifications

• 4+ years of experience in statistical programming and clinical trials.
• Strong background in SAS programming and statistical analysis.

Responsibilities

• Perform programming support across various projects and clients.
• Lead study team meetings and mentor junior team members.

Skills

SAS Programming

Statistical Techniques

Data Analysis

Clinical Trial Documentation

Education

BSc in Numerical Discipline

MSc in Numerical Discipline

PhD in Numerical Discipline

Tools

SAS

Job description

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

Client: Veramed

Location: Altrincham, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 4

Posted: 26.04.2025

Expiry Date: 10.06.2025

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 a Senior Statistical Programmer 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
• Review CDISC Validation reports
• Ensure standards are applied and adhered to
• Familiar with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis)
• Review project management documents
• Maintain study master files and audit-ready documents

General

• Lead study team meetings and present updates
• Share technical and scientific knowledge
• Ensure compliance with regulations and policies
• Build collaborative relationships with teams
• Mentor junior team members
• Contribute to training materials and process improvements

Qualifications:

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

What To Expect

• A supportive and friendly working environment
• Development opportunities and career support
• Unique company culture focused on staff management and relationship building
• Opportunity to develop skills and own your role