Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Cheltenham; Hybrid; GBP 50,000 - 75,000; Full time

Job summary

A leading company is seeking a Principal Statistical Programmer to provide programming support across various projects. This full-time position offers flexible working arrangements and opportunities for career growth, with responsibilities including data analysis, project management, and team leadership. Candidates should have a strong background in clinical drug development and SAS programming.

Benefits

Competitive package

Training and support for career growth

Flexible working arrangements

Qualifications

• Minimum 6 years of relevant industry experience required.
• Experience with clinical trial documents (protocols, CRFs).
• Ability to mentor and coach junior staff.

Responsibilities

• Review and author clinical trial documents and SAS programs.
• Line management of statisticians and programmers.
• Oversee key client projects ensuring timely delivery.

Skills

Understanding of clinical drug development

Proficiency in SAS

Data analysis

Project management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location: Cheltenham, UK

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 have an exciting opportunity for a Principal Statistical Programmer 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 across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory duties such as line or project management.

Key Responsibilities

The following tasks outline the scope of the position, which may vary based on business needs.

Technical

• Review clinical trial documents including 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
• Review and approve CDISC Validation reports
• Address data and standards issues appropriately
• Stay aware of emerging standards and their impact on trials
• Maintain proficiency in SAS and stay updated on developments
• Ensure study master files and audit-ready documents are maintained

People Management

• Line management of statisticians, programmers, and technical staff, overseeing performance
• Coach, mentor, and support staff career development and training
• Interview, onboard, and integrate new team members
• Provide technical leadership and coaching

Project Management

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

General

• Lead internal and client meetings effectively
• Present study updates internally and externally
• Share knowledge within the team and with colleagues
• Ensure compliance with policies and procedures
• Build collaborative relationships with teams and clients
• Share learnings across projects
• Develop and deliver internal technical training

Qualifications:

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

Additional Requirements

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

What to Expect:

• A supportive, friendly working environment for personal and professional growth
• Open management policy supporting career development
• A unique CRO approach to staff and project management
• Opportunities to own your role and develop skills