Principal Statistical Programmer - Remote, Office or Hybrid - UK

ZipRecruiter; Altrincham; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading clinical research organization is seeking a Principal Statistical Programmer to provide programming support across various clinical projects. This role involves line management of technical staff and project oversight while offering flexible working arrangements. Ideal candidates should have at least 6 years in the industry and a strong foundation in clinical trial processes and SAS programming.

Benefits

Training and professional development

Supportive management policy

Friendly working environment

Qualifications

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

Responsibilities

• Provide programming support across various projects and clients.
• Perform line management of statisticians and programmers.
• Oversee client projects and manage expectations.

Skills

Clinical trial document review

SAS programming

Project management

Team leadership

Education

BSc, MSc, or PhD in a numerical discipline

Job description

Job Description

Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and offering an industry-leading working environment with support and training for career growth.

We have an exciting opportunity for a Principal level Statistical Programmer to join us on a permanent basis in the UK. We can offer home and/or office working, training, support, and a competitive package.

The purpose of the role is to provide programming support to the statistics and programming department across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory roles (e.g., line management and/or project management).

Key Responsibilities

The tasks outlined below describe the scope of the position. The application of these tasks may vary based on current business needs.

Technical

• Perform 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 for datasets, TFLs, and macros, applying good programming practices
• Identify data issues and outliers
• Complete, review, and approve CDISC Validation tool reports
• Identify data and standards issues and resolve or escalate as appropriate
• Maintain awareness of emerging standards and their impact on ongoing and future trials
• Maintain proficiency in SAS and stay updated on developments
• Maintain study master file documents and other audit-ready documents

People Management

• Line management of statisticians, programmers, and other technical staff, responsible for overall performance
• Provide coaching and mentoring to achieve excellence
• Manage employee career development and ensure appropriate training
• Interview, onboard, and integrate new staff members effectively
• Provide technical leadership and coaching in programming

Project Management

• Oversee key client projects/portfolios, acting as Veramed Project Manager
• Maintain project plans
• Proactively manage resources, scope changes, and risks
• Ensure project delivery within budget
• Manage client expectations and resolve issues

General

• Lead internal and client study, project, and cross-functional team meetings effectively
• Present study updates internally and at client meetings
• Share scientific, technical, and practical knowledge within the team
• Ensure full compliance with internal and client policies, procedures, and training
• Build effective collaborative relationships with internal and client teams
• Share learnings across projects or studies
• Develop and deliver internal technical training where appropriate
• Lead process improvement initiatives

Minimum Qualification Requirements

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

Other Information/Additional Requirements

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

What to Expect:

• A warm, friendly working environment to thrive both personally and professionally
• A supportive, open-door management policy aiding your development and career progression
• A unique CRO doing things differently in managing staff, projects, and relationships
• The opportunity to own your role and develop your skills and experience