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

JR United Kingdom; Chelmsford; Hybrid; GBP 40,000 - 65,000; Full time

Job summary

A leading consultancy firm in the UK is looking for a Senior Statistical Programmer to join their dynamic team. The position offers flexible working arrangements and the chance to lead critical statistical programming projects that impact clinical trials. The ideal candidate will have a strong background in statistics, programming in SAS, and a passion for mentoring junior staff members in a supportive environment.

Benefits

Flexible working arrangements

Training and support provided

Opportunities for career growth

Qualifications

• Minimum 4 years of relevant experience.
• Degree in statistics or equivalent industry experience is essential.

Responsibilities

• Perform consistency reviews of clinical trial documents.
• Program and QC datasets and TFLs in SAS.
• Mentor junior team members and contribute to training materials.

Skills

Statistical Techniques

Programming in SAS

Data Checks & Exploration

Project Management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location:

Job Category: Other

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EU work permit required: Yes

Job Views:

4

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 are seeking Senior Statistical Programmers for a permanent role in the UK. We offer flexible working arrangements, training, support, and a competitive package.

The role involves providing programming support to the statistics and programming department across various projects, clients, and therapeutic areas.

Key Responsibilities

Technical

• Perform consistency reviews 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 adhered to
• Familiarity 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
• Present study updates internally and to clients
• Share knowledge within the team
• Ensure compliance with regulations and policies
• Build collaborative relationships
• Develop innovative ideas
• 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
• Open-door management to aid your development
• A unique CRO with innovative staff and project management
• Opportunities to develop your skills and experience