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

JR United Kingdom; Milton Keynes; Hybrid; GBP 45,000 - 65,000; Full time

Job summary

A leading company in statistics and programming consultancy is seeking a Senior Statistical Programmer. This role offers flexible working options (remote, office, hybrid) and focuses on programming tasks across various projects. The successful candidate will benefit from a supportive environment that emphasizes professional development and innovative ideas.

Benefits

Flexible working arrangements

Professional development opportunities

Supportive work environment

Unique company culture

Qualifications

• 4+ years of relevant experience is required.
• Experience with CDISC validation reports and compliance standards.
• Ability to mentor junior team members and lead meetings.

Responsibilities

• Provide programming support for clinical trial documents and datasets.
• Ensure compliance with regulations and maintain audit-ready documents.
• Lead study team meetings and facilitate knowledge sharing.

Skills

Statistical techniques

SAS

Data management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

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 work environment supporting career growth.

We have an exciting opportunity for Senior Statistical Programmers in the UK. We offer home, office, or hybrid 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 using SAS
• Program and QC datasets and TFLs following specifications
• Complete and review CDISC validation reports
• Ensure standards compliance
• Familiar with basic statistical techniques (e.g., t-test, ANOVA, regression, survival analysis)
• Review project management documents
• Maintain audit-ready study documents

General

• Lead study team meetings and present updates
• 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 relevant industry experience
• At least 4 years of relevant experience

What To Expect

• A supportive and friendly work environment
• Opportunities for professional development
• Unique company culture with strong staff management and relationship building
• Role ownership and skill development opportunities