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

JR United Kingdom; Bolton; Hybrid; 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 remote, office, or hybrid work arrangements, alongside a supportive environment that fosters professional development. The ideal candidate will have a strong background in statistical programming, particularly with SAS, and will contribute to various projects across therapeutic areas. With opportunities for mentorship and career progression, this position is perfect for those looking to make a significant impact in the clinical research field.

Benefits

Professional Development Opportunities

Supportive Work Environment

Career Progression

Mentorship Programs

Qualifications

• 4+ years of experience in statistical programming and clinical trials.
• Strong knowledge of SAS and statistical techniques.

Responsibilities

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

Skills

SAS Programming

Statistical Analysis

Data Quality Control

Clinical Trial Documentation

Team Collaboration

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), Bolton

Client: Veramed

Location:

Job Category: Other

EU work permit required: Yes

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

Veramed prides itself on providing high-quality statistics and programming consultancy, and offering an excellent working environment with support and training for career growth.

We are seeking a Senior Statistical Programmer for a permanent role in the UK, with options for home, office, or hybrid work, along with 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 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, ensuring good programming practices
• 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
• Ensure compliance with legislation, regulations, policies, and procedures
• Build collaborative relationships with team members
• Develop innovative ideas and share when appropriate
• Mentor junior team members
• Contribute to internal training materials 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
• Opportunities for professional development and career progression
• Unique CRO culture focused on staff management, projects, and relationships
• Role ownership and skill development opportunities