Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Liverpool; Remote; GBP 50,000 - 75,000; Full time

Job summary

A leading consultancy in statistics and programming is looking for a Principal Statistical Programmer to join their team in Liverpool. This role offers a supportive environment, flexible working options, and a competitive salary. The position involves comprehensive programming support across projects, managing teams, and ensuring compliance in clinical trials.

Benefits

Supportive work environment

Opportunities for skill development

Flexible working options

Open-door management policy

Qualifications

• At least 6 years of relevant experience in statistical programming.
• Strong proficiency in SAS programming and data management.
• Experience in clinical trial processes and regulatory standards.

Responsibilities

• Review clinical trial documents and develop programming specifications.
• Provide programming support across various projects and therapeutic areas.
• Manage resources and client expectations within project management.

Skills

Data management

Programming in SAS

Statistical analysis

Clinical trial documentation review

Project management

Education

BSc, MSc, or PhD in a numerical discipline

Job description

Social network you want to login/join with:

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

Client: Veramed

Location: Liverpool, 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, and offering an excellent working environment with support and training for career growth.

We are seeking a Principal Statistical Programmer for a permanent role in the UK. The position offers flexible working options, training, support, and a competitive package.

The role involves providing programming support across various projects and therapeutic areas. The Senior or Principal Programmer may also have supervisory responsibilities, including line and project management.

Key Responsibilities

The tasks include, but are not limited to:

• Review of clinical trial documents such as protocols, SAPs, CRFs, and CSRs
• Authoring, reviewing, and approving study TFL shells and dataset specifications
• Authoring, validating, and documenting SAS programs, ensuring good programming practices
• Identifying data issues and outliers
• Reviewing CDISC Validation reports
• Resolving data and standards issues or escalating as needed
• Staying updated on emerging standards and their impact on trials
• Maintaining proficiency in SAS and awareness of developments
• Managing study documentation to ensure audit readiness

People Management

Line management of statisticians, programmers, and technical staff, including coaching, mentoring, and career development. Responsible for onboarding new staff and providing technical leadership.

Project Management

Oversee key projects, maintain project plans, manage resources, scope, risks, and budgets, and handle client expectations and issues.

General Responsibilities

Lead meetings, present updates, share knowledge, ensure compliance, build collaborative relationships, and develop internal training.

Qualifications

BSc, MSc, or PhD in a numerical discipline or relevant industry experience, with 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 with innovative staff and project management
• Opportunities for role ownership and skill development