Principal Statistical Programmer - Remote, Office or Hybrid - UK

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

Job summary

A leading consultancy in the UK is seeking a Principal Statistical Programmer to join their team. This role offers flexible working arrangements and focuses on programming support, project management, and team leadership in clinical trial environments. Ideal candidates will possess a strong background in statistical programming, particularly using SAS, and a proven track record in managing projects and teams. The company emphasizes career growth, training, and a supportive work environment.

Benefits

Flexible working arrangements

Training and support

Career development tools

Qualifications

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

Responsibilities

• Review clinical trial documents and develop SAS programs.
• Manage statisticians and programmers, oversee project management.
• Ensure compliance and lead team meetings.

Skills

Statistical programming

Data analysis

Project management

People management

Education

BSc, MSc, or PhD in a numerical discipline

Tools

SAS

Job description

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

Client:

Veramed

Location:

UK, Chelmsford

Job Category:

Other

EU work permit required: Yes

Job Views: 9

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 role in the UK. The position offers 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 perform supervisory duties such as line management and project management.

Key Responsibilities

Technical

• Review clinical trial documents including 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
• Review and approve CDISC Validation reports
• Address data and standards issues and escalate as needed
• Stay updated on emerging standards and their impact on trials
• Maintain proficiency in SAS and stay informed of developments
• Ensure audit readiness of study master files and related documents

People Management

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

Project Management

• Oversee client projects and portfolios, acting as Project Manager
• Maintain project plans and manage resources, scope, and risks
• Ensure projects are delivered within budget
• Manage client expectations and resolve issues

General

• Lead study, project, and team meetings effectively
• Present updates internally and to clients
• Share knowledge within the team
• Ensure compliance with policies and procedures
• Build collaborative relationships with team members
• Share learnings across projects
• Develop and deliver internal technical training

Qualifications:

• BSc, MSc, or PhD in a numerical discipline or equivalent 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 fostering personal and professional growth
• Open-door management policy and career development tools
• A unique CRO culture emphasizing staff management, project handling, and industry relationships
• Opportunities to own your role and develop your skills