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

JR United Kingdom; West Midlands Combined Authority; Remote; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Senior Statistical Programmer to join their dynamic team. This role offers the flexibility of home and office working while providing a supportive environment for personal and professional growth. You will be involved in programming support across various projects, ensuring high-quality standards in clinical trial documentation and data analysis. With opportunities to mentor junior team members and contribute to innovative ideas, this position is perfect for those looking to make a significant impact in the field of statistical programming. Join a forward-thinking company that values collaboration and career development.

Benefits

Home Office Flexibility

Training and Support

Career Growth Opportunities

Friendly Working Environment

Qualifications

• 4+ years of relevant industry experience in statistical programming.
• Experience with clinical trial documentation and data analysis.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Program and QC datasets and TFLs in SAS.
• Lead study team meetings and mentor junior 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), London (West End)

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Client:

Veramed

Location:

London (West End), United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

26.04.2025

Expiry Date:

10.06.2025

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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 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 reviews of clinical trial documents such as protocols, SAPs, CRFs, and 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 and good practices.
• Review CDISC Validation reports.
• Ensure standards are applied correctly.
• Familiar with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis).
• Review project management documents.
• Maintain audit-ready study master files and related documents.

General

• Lead study team meetings effectively.
• Present study updates internally and to clients.
• Share knowledge within the team and with colleagues.
• Work in compliance with applicable laws, regulations, and policies.
• Build collaborative relationships with internal and client teams.
• Develop innovative ideas and share them appropriately.
• Mentor junior team members.
• Contribute to internal training and process improvements.

Qualifications:

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

What To Expect

• A friendly working environment supporting personal and professional growth.
• Supportive management fostering career development.
• A unique CRO approach to staff and project management.
• Opportunities to own your role and develop skills.