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

JR United Kingdom; York; Hybrid; GBP 40,000 - 70,000; Full time

Job summary

A leading consultancy is looking for a Senior Statistical Programmer to join their team in the UK with remote/hybrid working options. The role involves providing programming support across various projects and therapeutic areas, with opportunities for professional development and skill enhancement in a collaborative environment.

Benefits

Supportive working environment

Opportunities for personal development

Innovative management approaches

Qualifications

• 4+ years of relevant experience in statistical programming.
• Experience with CDISC standards and clinical trial documentation.

Responsibilities

• Perform clinical trial document reviews and ensure quality standards.
• Lead study team meetings and mentor junior staff.
• Program datasets and create analysis deliverables.

Skills

SAS programming

Basic statistical techniques

Data 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), York

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, offering home and/or office working, 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 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 tools like frequencies and histograms
• Program and QC datasets and TFLs in SAS following specifications
• Complete and review CDISC Validation reports
• Ensure standards are adhered to
• Familiar with basic statistical techniques (t-test, ANOVA, regression, survival analysis)
• Review project management documents
• Maintain audit-ready study master files

General

• Lead and participate in study team meetings
• Present updates to internal and client teams
• Share knowledge within the team
• Ensure compliance with legislation, 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 working environment
• Management that supports your development
• A unique CRO with innovative management approaches
• Opportunities to own your role and develop skills