Principal Statistical Programmer - Remote, Office or Hybrid - UK

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

Job summary

A leading consultancy is seeking a Principal Statistical Programmer in Brighton, offering a flexible working environment. The role entails providing programming support, managing technical staff, and overseeing various client projects in a dynamic and innovative setting.

Benefits

Supportive and friendly work environment

Open-door management policy

Opportunities for role ownership and skill development

Qualifications

• At least 6 years of relevant industry experience.
• Understanding of clinical drug development and study designs.

Responsibilities

• Provide programming support across various projects and clients.
• Manage staff performance and provide technical leadership.
• Oversee client projects, ensuring timely delivery and compliance.

Skills

Clinical Trial Documentation

SAS Programming

Data Issue Resolution

People Management

Project Management

Education

BSc, MSc, or PhD in a numerical discipline or relevant industry experience

Job description

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

Client: Veramed

Location: Brighton, 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, along with an industry-leading working environment supporting career growth.

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

The role involves providing programming support across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also undertake supervisory responsibilities, 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, CSRs)
• Author, review, and approve study TFL shells and dataset specifications
• Develop and validate SAS programs for datasets, TFLs, and macros, following good programming practices
• Identify data issues and outliers
• Review and approve CDISC Validation reports
• Resolve or escalate data and standards issues
• Stay informed about emerging standards and their impact on trials
• Maintain SAS proficiency and stay updated on developments
• Keep study master files and audit-ready documents

People Management

• Manage statisticians, programmers, and technical staff; oversee performance
• Coach and mentor staff for excellence
• Handle onboarding and training of new staff
• Provide technical leadership and coaching

Project Management

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

General

• Lead study, project, and team meetings
• Present updates internally and to clients
• Share knowledge and provide internal training
• Ensure compliance with policies and procedures
• Build collaborative relationships internally and with clients
• Share learnings across projects
• Develop and deliver technical training

Qualifications:

• BSc, MSc, or PhD in a numerical discipline or relevant industry experience
• At least 6 years of relevant industry 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 fostering development
• A unique CRO with innovative staff and project management
• Opportunities for role ownership and skill development