Jobs in Ipswich, United Kingdom

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Client:

Veramed

Location:

UK, Ipswich

Job Category:

Other

EU work permit required: Yes

Job Views:

4

Posted:

26.06.2025

Expiry Date:

10.08.2025

Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working environment that supports career growth.

We are seeking a Principal Statistical Programmer for a permanent role in the UK, offering home and/or office work, training, support, and a competitive package.

The role involves supporting the statistics and programming department across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also have supervisory responsibilities, such as line or project management.

The tasks below outline the scope of the role, which may vary based on business needs.

• 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 following good programming practices
• Identify data issues and outliers
• Review and approve CDISC validation reports
• Address data and standards issues appropriately
• Stay informed about emerging standards and their impact on trials
• Maintain proficiency in SAS and stay updated on developments
• Keep study master files and other audit-ready documents

• Manage statisticians, programmers, and technical staff, ensuring performance
• Coach and mentor staff for excellence
• Oversee staff onboarding and training
• Provide technical leadership and coaching

• Manage client projects and portfolios
• Serve as Veramed Project Manager for client accounts
• Maintain project plans, manage resources, scope, risks, and budgets
• Manage client expectations and resolve issues

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

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

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

• A supportive and friendly work environment for personal and professional growth
• Open-door management policy for development and career advancement
• A unique CRO approach to staff and project management
• Opportunities to own your role and develop skills