Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Wolverhampton; Hybrid; GBP 50,000 - 80,000; Full time

Job summary

A leading consultancy firm in Wolverhampton seeks a Principal Statistical Programmer. This role involves overseeing programming tasks, managing client projects, and providing technical leadership within a supportive environment. Candidates should have a numerical degree and extensive industry experience, with excellent SAS and project management skills.

Benefits

Supportive and friendly working environment

Opportunities for personal and professional growth

Open-door management policy

Innovative staff management approaches

Qualifications

• Minimum 6 years relevant industry experience.
• Strong understanding of clinical drug development.

Responsibilities

• Provide programming support across various projects.
• Manage projects including plans, resources, and client expectations.
• Line management of statistical and programming staff.

Skills

Data Analysis

Programming

Project Management

SAS Proficiency

Technical Leadership

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location: Wolverhampton, UK

Job Category: Other

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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 position in the UK, offering home and/or office work, 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

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

Technical

• Review clinical trial documents (protocols, SAPs, CRFs, CSRs)
• Author, review, and approve study TFL shells and dataset specifications
• Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices
• Identify data issues and outliers
• Complete, review, and approve CDISC Validation reports
• Resolve or escalate data and standards issues
• Stay informed on emerging standards and their impact on trials
• Maintain proficiency in SAS and stay updated with developments
• Maintain study master files and audit-ready documents

People Management

• Line management of statisticians, programmers, and technical staff
• Provide coaching, mentoring, and career development for staff
• Recruit, onboard, and integrate new team members
• Offer technical leadership and coaching

Project Management

• Oversee client projects and portfolios
• Manage project plans, resources, scope, and risks
• Ensure project delivery within budget
• Manage client expectations and resolve issues

General

• Lead internal and client meetings effectively
• Present study updates internally and externally
• Share scientific, technical, and practical knowledge
• Ensure compliance with policies and procedures
• Build collaborative relationships with internal and external teams
• 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 relevant industry experience

Additional Requirements

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

What to Expect:

• A supportive, friendly working environment for personal and professional growth
• Open-door management policy encouraging development
• A unique CRO with innovative staff and project management approaches
• Opportunities to own your role and develop skills