Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Stoke-on-Trent; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

Une entreprise leader dans le domaine des statistiques et de la programmation offre un poste de Programmeur Statistique Principal. Ce rôle flexible, qui peut être effectué à distance, en hybride ou au bureau, inclut la gestion d'équipe, le support de projets, ainsi qu'une culture unique et collaborative propice au développement des compétences.

Benefits

Environnement de travail soutenant

Culture unique au sein du CRO

Opportunités de développement des compétences

Qualifications

• Au moins 6 ans d'expérience pertinente.
• Compréhension du développement clinique et des conceptions d'études.
• Expérience en gestion d'équipe et leadership technique.

Responsibilities

• Revoir des documents d'essai clinique et approuver des spécifications de données.
• Gérer les projets clients et maintenir la documentation.
• Former et diriger les statisticiens et programmeurs.

Skills

SAS

Programmation

Gestion de projet

Gestion d'équipe

Analyse statistique

Education

BSc, MSc, or PhD in a numerical discipline

Job description

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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Stoke-on-Trent

Client: Veramed

Location: Stoke-on-Trent, 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, 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 in the UK. The role offers remote, hybrid, or office working, training, support, and a competitive package.

The role involves providing programming support across various projects, clients, and therapeutic areas, with potential supervisory responsibilities such as line or project management.

Key Responsibilities

The tasks include:

• Review of clinical trial documents (protocols, SAPs, CRFs, CSRs)
• Authoring, reviewing, and approving study TFL shells and dataset specifications
• Authoring, validating, and documenting SAS programs
• Data issue identification and resolution
• Reviewing CDISC Validation reports
• Maintaining proficiency in SAS and awareness of standards
• Maintaining audit-ready study documentation

People Management

Line management of statisticians and programmers, coaching, mentoring, onboarding, and technical leadership.

Project Management

Overseeing client projects, maintaining project plans, managing resources, scope, risks, budgets, and client expectations.

General

Leading meetings, presenting updates, sharing knowledge, ensuring compliance, building relationships, sharing learnings, and developing internal training.

Qualifications

BSc, MSc, or PhD in a numerical discipline or relevant industry experience, with at least 6 years of relevant experience.

Additional Requirements

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

What to Expect

• A supportive and friendly work environment
• Management that supports your development
• Unique CRO culture
• Opportunities for role ownership and skill development