Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Coventry; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading consultancy in statistical programming is seeking a Principal Statistical Programmer in Coventry. This role offers a hybrid work environment, focusing on programming support, project management, and team leadership. Successful candidates will benefit from a supportive atmosphere, opportunities for skill development, and a competitive salary package.

Benefits

Supportive work environment

Open-door management policy

Opportunities for career growth

Qualifications

• Minimum 6 years of relevant industry experience.
• Experience in clinical drug development and study designs.

Responsibilities

• Provide programming support across various projects.
• Line manage statisticians and programmers.
• Oversee key client projects and maintain project plans.

Skills

SAS programming

Data analysis

Project management

Team leadership

Clinical trial knowledge

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location: Coventry, 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, support, and training for career growth.

We are seeking a Principal Statistical Programmer for a permanent role in the UK, offering home and/or office working, 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, such as line management or project management.

Key Responsibilities

The following tasks outline the scope of the role. Tasks may vary based on current business needs.

Technical

• Review clinical trial documents (protocols, SAPs, CRFs, CRSs)
• Author, review, and approve study TFL shells and dataset specifications
• Develop, validate, and document SAS programs, ensuring good programming practices
• Identify data issues and outliers
• Review and approve CDISC Validation reports
• Resolve data and standards issues or escalate as needed
• Stay informed about emerging standards and their impact on trials
• Maintain proficiency in SAS and stay updated with 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 employee career development and training
• Onboard and integrate new staff members effectively
• Provide technical leadership and coaching

Project Management

• Oversee key client projects and portfolios
• Act as Veramed Project Manager on 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, technical, and practical knowledge
• Ensure compliance with policies, procedures, and training
• Build collaborative relationships with internal and client teams
• Share learnings across projects
• Develop and deliver internal technical training

Qualifications:

• BSc, MSc, or PhD in a numerical discipline or relevant industry experience
• Minimum 6 years of relevant industry experience

Additional Requirements

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

What to Expect:

• A supportive and friendly work environment for personal and professional growth
• Open-door management policy to aid development
• A unique CRO approach to staff, projects, and industry relationships
• Opportunities to own your role and develop skills