Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Crawley; Hybrid; GBP 55,000 - 80,000; Full time

Job summary

A leading company in statistics and programming consultancy is seeking a Principal Statistical Programmer for a permanent role in Crawley, UK. This position offers flexible working options and requires a minimum of 6 years of industry experience. Key responsibilities include programming support, overseeing client projects, and line management of technical staff.

Benefits

Flexible working options

Training and support

Competitive package

Qualifications

• At least 6 years of industry experience.
• Proficiency in clinical trial documentation.

Responsibilities

• Provide programming support across various projects.
• Manage staff onboarding and training.
• Oversee client projects and portfolios.

Skills

SAS

Data Analysis

Project Management

Statistical Programming

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Crawley, West Sussex

Client: Veramed

Location: Crawley, West Sussex, 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. We offer 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 management and project management.

Key Responsibilities

The tasks below outline the scope of the role, which may vary based on business needs.

Technical

• Review clinical trial documents such as protocols, SAPs, CRFs, 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 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.
• Keep study documentation audit-ready.

People Management

• Line manage statisticians, programmers, and technical staff, overseeing performance.
• Coach and mentor staff to achieve excellence.
• Manage staff onboarding and training.
• Provide technical leadership and coaching.

Project Management

• Oversee client projects and portfolios.
• Act as Project Manager for client accounts.
• Maintain project plans and 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 to clients.
• Share scientific and technical knowledge.
• Ensure compliance with policies and procedures.
• Build collaborative relationships internally and with clients.
• 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 friendly working environment supporting personal and professional growth.
• Supportive management with development tools.
• A unique CRO focused on innovative staff and project management.
• Opportunity to own your role and develop skills.