Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Southampton; Hybrid; GBP 45,000 - 65,000; Full time

Job summary

A leading clinical research organization is seeking a Principal Statistical Programmer in Southampton, UK. The position offers flexibility with remote or hybrid working options. Responsibilities include programming, project management, and team leadership, making it ideal for candidates with significant industry experience and a strong statistical background.

Benefits

Supportive working environment

Open-door management policy

Opportunities for personal development

Qualifications

• At least 6 years of industry experience in a statistical programming role.
• Strong understanding of clinical trial documents and SAS proficiency.

Responsibilities

• Review clinical trial documents and author study specifications.
• Manage project plans and oversee key client projects.
• Coach and mentor staff for excellence in performance.

Skills

SAS programming

Data management

Statistical analysis

Clinical trial understanding

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location: Southampton, 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, offering home and/or office working, training, and a competitive package.

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

Key Responsibilities:

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, ensuring good programming practices
• Identify data issues and outliers
• Review CDISC validation reports
• Resolve data and standards issues
• Stay updated on emerging standards and their impact
• Maintain SAS proficiency and awareness of developments
• Ensure audit-ready study documentation

People Management:

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

Project Management:

• Oversee key client projects and portfolios
• Manage project plans, 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 develop internal training
• Comply 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 experience
• At least 6 years of industry experience

Additional Requirements:

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

What to Expect:

• A supportive, friendly working environment
• Open-door management policy for development
• A unique CRO with innovative management and relationship-building
• Opportunities to own your role and develop skills