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

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

Job summary

A leading consultancy in the UK is seeking a Senior Statistical Programmer to provide essential programming support across various projects. This role offers flexible working options, a commitment to employee development, and the chance to work within a supportive team environment. The ideal candidate will have a strong background in statistics and programming, alongside excellent communication skills to collaborate effectively with clients and colleagues.

Benefits

Supportive working environment

Training and development opportunities

Flexible working options

Qualifications

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

Responsibilities

• Perform consistency review of clinical trial documents.
• Program and QC datasets and TFLs in SAS.
• Lead internal and client study meetings effectively.

Skills

Consistency review

Data analysis

SAS programming

Statistical techniques

Mentoring

Education

BSc in a numerical discipline

MSc in a numerical discipline

PhD in a numerical discipline

Job description

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

Client:

Veramed

Location:

Luton, Bedfordshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

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 have an exciting opportunity for Senior Statistical Programmers 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 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, 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.
• Complete and 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 audit-ready study master files and related documents.

General

• Lead internal and client study meetings effectively.
• Present study updates internally and to clients.
• Share knowledge within the team and with colleagues.
• Work in compliance with legislation, regulations, policies, and procedures.
• Build collaborative relationships internally and externally.
• 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 supportive and friendly working environment.
• Management policies that support your development.
• A unique CRO approach to staff, projects, and relationships.
• Opportunities to own your role and develop skills.