Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Derby; Remote; GBP 50,000 - 80,000; Full time

Job summary

A leading analytical consultancy in the UK is seeking a Principal Statistical Programmer to join their dynamic team in Derby. This permanent position offers flexible work arrangements, a dedication to professional development, and a competitive salary package. The ideal candidate will work on diverse projects across therapeutic areas while managing a team of statisticians and programmers.

Benefits

Professional development opportunities

Supportive working environment

Flexible working arrangements

Qualifications

• 6+ years of relevant experience in statistical programming.
• Proficient in SAS with strong understanding of clinical trial processes.
• Possess a numerical degree or relevant industry experience.

Responsibilities

• Develop and validate SAS programs for clinical trial datasets.
• Manage junior staff and oversee project plans.
• Lead technical delivery and ensure document compliance.

Skills

Data Analysis

Statistical Programming

Technical Leadership

Project Management

Education

BSc, MSc, or PhD in a numerical discipline

Tools

SAS

Job description

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

Client: Veramed

Location: Derby, 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 position offers flexible working arrangements, training, support, and a competitive package.

The role involves providing programming support across various projects, clients, and therapeutic areas, with potential supervisory responsibilities.

Key Responsibilities

The tasks below outline the scope; actual duties 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, 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
• Address data and standards issues appropriately
• Stay updated on emerging standards and their impact on trials
• Maintain proficiency in SAS and stay informed about developments
• Ensure study documentation is audit-ready

People Management

• Manage statisticians, programmers, and technical staff, overseeing 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
• Manage project plans, resources, scope, and risks
• Deliver projects within budget
• Manage client expectations and resolve issues

General

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

Qualifications

BSc, MSc, or PhD in a numerical discipline or relevant industry experience, with 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 working environment
• Opportunities for professional development
• A unique CRO culture focused on staff management and relationship building
• Ownership of your role and skill development