Principal Statistical Programmer - Remote, Office or Hybrid - UK

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

Job summary

A leading company in statistical programming is seeking a Principal Statistical Programmer to join their team in Leigh, UK. Offering flexible working arrangements, this permanent role involves programming support for diverse projects and includes supervisory responsibilities. The ideal candidate will have a numerical degree and at least 6 years of relevant experience, with opportunities for professional development in a supportive environment.

Benefits

Flexible working options

Training and support

Competitive package

Qualifications

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

Responsibilities

• Provide programming support across various projects and therapeutic areas.
• Manage statisticians and technical staff, overseeing performance.
• Oversee key client projects and maintain project plans.

Skills

Programming

SAS

Data Analysis

Team Management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Leigh, Greater Manchester

Client: Veramed

Location: 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 excellent working environment supporting career growth.

We are seeking a Principal Statistical Programmer for a permanent role in the UK. The role offers flexible working options, 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 have supervisory responsibilities, including line and project management.

Key Responsibilities

Technical

• Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs
• Author, review, and approve study TFL shells and dataset specifications
• Develop and validate SAS programs, ensuring good programming practices
• Identify data issues and outliers
• Review CDISC validation reports
• Resolve data and standards issues or escalate as needed
• Stay informed about emerging standards and their impact on trials
• Maintain SAS proficiency and stay updated on developments
• Maintain study documentation for audits

People Management

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

Project Management

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

General

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

Qualifications:

• BSc, MSc, or PhD in a numerical discipline or relevant industry 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 and friendly working environment
• Open-door management policy for development
• A unique CRO with innovative staff and project management
• Opportunities to own and develop your role