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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Brighton
Client: Veramed
Location: Brighton, 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. The role offers 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 undertake supervisory responsibilities, such as line or project management.
Key Responsibilities
The tasks below outline the scope of the role, 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 and validate SAS programs for datasets, TFLs, and macros, following good programming practices
* Identify data issues and outliers
* Review and approve CDISC Validation reports
* Resolve or escalate data and standards issues
* Stay informed about emerging standards and their impact on trials
* Maintain SAS proficiency and stay updated on developments
* Keep study master files and audit-ready documents
People Management
* Manage statisticians, programmers, and technical staff; oversee performance
* Coach and mentor staff for excellence
* Handle 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
* Present updates internally and to clients
* Share knowledge and provide internal training
* Ensure compliance with policies and procedures
* Build collaborative relationships internally and with clients
* Share learnings across projects
* Develop and deliver technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or relevant industry 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 and friendly work environment
* Open-door management policy fostering development
* A unique CRO with innovative staff and project management
* Opportunities for role ownership and skill development
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