Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Chester; Hybrid; GBP 60,000 - 90,000; Full time

Job summary

A leading consultancy is seeking a Principal Statistical Programmer for a permanent role based in Chester, UK. This position offers flexibility with remote and hybrid work options, and involves overseeing clinical trial projects, providing technical leadership, and supporting statistical programming. Ideal candidates will have substantial experience and a strong educational background in relevant disciplines, alongside excellent people management skills.

Benefits

Supportive work environment

Training and career development

Flexible working options

Qualifications

• Minimum 6 years of relevant experience in statistical programming.
• Understanding of clinical drug development and study designs.

Responsibilities

• Review and approve clinical trial documentation.
• Manage staff and oversee key client projects.
• Ensure compliance and lead project meetings.

Skills

SAS proficiency

Project Management

People Management

Statistical Analysis

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Chester

Client: Veramed

Location: Chester, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

4

Posted:

26.06.2025

Expiry Date:

10.08.2025

Job Description:

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

We are seeking a Principal Statistical Programmer for a permanent position in the UK. The role offers home and/or office working, training, support, and a competitive package.

The main purpose is to support the statistics and programming department across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory roles such as line or project management.

Key Responsibilities

The tasks below outline the scope of the role, which may vary based on business needs.

Technical

• Review clinical trial documents (protocols, SAPs, CRFs, CRSs)
• Author, review, and approve study TFL shells and dataset specifications
• Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices
• Identify data issues and outliers
• Complete, review, and approve CDISC Validation reports
• Resolve or escalate data and standards issues
• Stay updated on emerging standards and their impact
• Maintain SAS proficiency and awareness of developments
• Keep study master files and audit-ready documents

People Management

• Line management of statisticians, programmers, and technical staff
• Coach and mentor staff for excellence
• Manage employee career development and training
• Onboard new staff members
• Provide technical leadership and coaching

Project Management

• Oversee key client projects and portfolios
• Serve as Veramed Project Manager
• Maintain project plans
• Manage resources, scope, and risks proactively
• Ensure projects are delivered within budget
• Manage client expectations and resolve issues

General

• Lead internal and client meetings effectively
• Present study updates internally and externally
• Share technical and scientific knowledge
• Ensure compliance with policies and procedures
• Build collaborative relationships
• Share learnings across projects
• Develop internal technical training

Qualifications:

• BSc, MSc, or PhD in a numerical discipline or equivalent industry experience
• At least 6 years of relevant experience

Additional Requirements

• Understanding of clinical drug development, disease areas, endpoints, and study designs

What to Expect:

• A supportive and friendly work environment
• Open-door management policy for development
• A unique CRO approach to staff and project management
• Opportunity to own your role and develop skills