Principal Statistical Programmer - Remote, Office or Hybrid - UK

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

Job summary

A leading company in clinical programming consultancy is seeking a Principal Statistical Programmer for a remote, office, or hybrid role in London. This position involves overseeing various programming tasks, managing projects, and providing mentorship to a team, with a focus on quality and compliance in clinical trials. Ideal candidates will possess strong SAS programming skills and have significant industry experience, thriving in a supportive environment that encourages professional growth.

Benefits

Supportive working environment

Training and career development

Qualifications

• 6+ years of relevant industry experience required.
• Understanding of clinical drug development and study designs.

Responsibilities

• Provide programming support across various projects and clients.
• Supervise and mentor abilities for team members.
• Manage key client projects and ensure timely delivery.

Skills

Programming in SAS

Clinical trial document review

Data management

Project management

Coaching and mentoring

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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

Client: Veramed

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 6

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 with support and training for career growth.

We have an exciting opportunity for a Principal level Statistical Programmer in the UK. We offer 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 supervise (e.g., line management and/or project management).

Key Responsibilities

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

Technical

• Review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author, review, and approve study TFL shells and dataset specifications
• Author, validate, and document SAS programs, applying good programming practices
• Identify data issues and outliers
• Complete, review, and approve CDISC Validation reports
• Resolve or escalate data and standards issues
• Maintain proficiency in SAS and stay updated on developments
• Maintain study master file documents for audit readiness

People Management

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

Project Management

• Oversee key client projects and portfolios
• Maintain project plans
• Manage resources, scope changes, and risks proactively
• Ensure projects are delivered within budget
• Manage client expectations and resolve issues

General

• Lead internal and client study and project meetings
• Present study updates internally and to clients
• Share scientific, technical, and practical knowledge
• Ensure compliance with policies and procedures
• 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
• 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 and friendly working environment
• Open-door management policy fostering development
• A unique CRO approach to staff and project management
• Opportunities to own your role and develop skills