Principal Statistical Programmer - Remote, Office or Hybrid - UK

JR United Kingdom; Worcester; Hybrid; GBP 60,000 - 85,000; Full time

Job summary

Une entreprise d'analyse de données de premier plan recherche un Principal Statistical Programmer pour rejoindre son équipe en offrant des opportunités de travail à distance, de bureau ou hybride. Ce rôle comprend des responsabilités de gestion de projet, de supervision du personnel technique, et la nécessité de rester à jour sur les normes en matière de données. Une solide formation en statistiques et au moins 6 ans d'expérience sont nécessaires pour garantir la qualité des livrables dans un environnement stimulant et collaboratif.

Benefits

Environnement de travail collaboratif

Opportunités de développement de carrière

Formation technique interne

Qualifications

• Minimum 6 ans d'expérience dans l'industrie.
• Compréhension du développement de médicaments et des conceptions d'études.

Responsibilities

• Fournir un soutien en programmation à divers projets et clients.
• Gérer des statisticiens et des programmeurs, superviser leurs performances.
• Agir en tant que chef de projet sur des comptes clients.

Skills

Leadership

Analyse de données

Gestion de projet

Compétences SAS

Education

BSc, MSc ou PhD en discipline numérique

Job description

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

Client:

Veramed

Location:

Worcester, 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 supporting 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 perform supervisory duties, including line and project management.

Key Responsibilities

The following tasks outline the role's scope, which may vary based on business needs.

Technical

• Review clinical trial documents (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
• Identify data issues and outliers
• Review CDISC Validation tool reports
• Resolve data and standards issues or escalate as needed
• Stay informed on emerging standards and their impact
• Maintain proficiency in SAS and stay updated on 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 hiring, onboarding, and training of new staff
• Provide technical leadership and coaching

Project Management

• Oversee client projects and portfolios
• Act as Project Manager on client accounts
• Maintain project plans and manage resources, scope, and risks
• Ensure project delivery within budget
• Manage client expectations and resolve issues

General

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

Qualifications:

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

Additional Requirements

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

What to Expect:

• A supportive, friendly working environment
• Management that fosters development and career growth
• A unique CRO approach to managing staff and projects
• Opportunities to own your role and develop skills