Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Bolton; Hybrid; GBP 50,000 - 75,000; Full time

Job summary

A leading consultancy firm is seeking a Principal Statistical Programmer for a flexible role in the UK. Responsibilities include managing projects, supervising staff, and providing programming support in a dynamic, supportive environment aimed at personal and professional growth.

Benefits

Flexible working arrangements

Training and support

Competitive salary package

Qualifications

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

Responsibilities

• Provide programming support across various projects.
• Manage statisticians, programmers, and technical staff.
• Oversee client projects, ensuring delivery within budget.

Skills

SAS programming

Data analysis

Project management

Statistical analysis

Team leadership

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location: Bolton, Greater Manchester, 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 work environment that supports career growth.

We are seeking a Principal level Statistical Programmer for a permanent role in the UK. We offer flexible working arrangements, 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 such as protocols, SAPs, CRFs, and 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 as appropriate
• Stay updated on emerging standards and their impact on trials
• Maintain proficiency in SAS and stay informed about developments
• Ensure study documents are audit-ready

People Management

• Manage statisticians, programmers, and technical staff, overseeing their performance
• Coach and mentor staff to achieve excellence
• Handle onboarding and training of new staff
• Provide technical leadership and coaching

Project Management

• Oversee 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 internal and client meetings effectively
• Present updates internally and externally
• Share knowledge within the team and with colleagues
• Ensure compliance with policies and procedures
• Build collaborative relationships with 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 friendly working environment for personal and professional growth
• Supportive management to aid your development
• A unique CRO approach to staff and project management
• Opportunities to own your role and develop your skills