Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Hemel Hempstead; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading statistical consultancy offers an exciting opportunity for a Principal Statistical Programmer in Hemel Hempstead, UK. The role includes programming, project management, and team leadership in a supportive and dynamic environment. Candidates should have extensive experience and a relevant degree alongside an understanding of clinical development.

Benefits

Supportive work environment

Training and development opportunities

Qualifications

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

Responsibilities

• Provide programming support across various projects.
• Supervise staff or projects as needed.
• Develop, validate, and document SAS programs.

Skills

SAS programming

Data analysis

Project management

People management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Hemel Hempstead

Client: Veramed

Location: Hemel Hempstead, 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, support, and training for career growth.

We have an exciting opportunity for a Principal level Statistical Programmer 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 supervise staff or projects.

Key Responsibilities

The following tasks outline the scope of the position, 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, ensuring good programming practices
• Identify data issues and outliers
• Complete and review CDISC Validation reports
• Resolve or escalate data and standards issues
• Stay informed of emerging standards and their impact
• Maintain SAS proficiency and awareness of developments
• Keep study master files audit-ready

People Management

• Manage statisticians, programmers, and technical staff, overseeing performance
• Coach and mentor staff for excellence
• Recruit, onboard, and integrate new team members
• Provide technical leadership and coaching

Project Management

• Manage client projects and portfolios
• Maintain project plans
• Manage resources, scope, and risks proactively
• Deliver projects within budget
• Manage client expectations and resolve issues

General

• Lead study, project, and team meetings
• Present updates internally and to clients
• Share knowledge within the team
• 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 relevant 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 experience in staff and project management
• Opportunities to own your role and develop skills