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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Swindon, Wiltshire
Client: Veramed
Location: Swindon, Wiltshire, 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 excellent working environment supporting career growth.
We are seeking a Principal Statistical Programmer for a permanent position 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 following tasks outline the scope of the role, which may vary based on business needs:
Technical
* Review clinical trial documents including protocols, SAPs, CRFs, and CSRs
* Author, review, and approve study TFL shells and dataset specifications
* Develop, validate, and document SAS programs for datasets, TFLs, and macros, adhering to good programming practices
* Identify data issues and outliers
* Complete, review, and approve CDISC Validation reports
* Resolve data and standards issues or escalate as needed
* Stay informed about emerging standards and their impact on trials
* Maintain proficiency in SAS and stay updated on developments
* Ensure study documentation is audit-ready
People Management
* Manage statisticians, programmers, and technical staff, overseeing their performance
* Coach and mentor staff to achieve excellence
* Handle onboarding and integration of new team members
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios
* 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 effectively
* Present updates internally and to clients
* Share knowledge within the team and with colleagues
* Ensure compliance with policies and procedures
* Build collaborative relationships internally and externally
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications
BSc, MSc, or PhD in a numerical discipline or relevant industry experience; at least 6 years of relevant experience.
Additional Requirements
Understanding of clinical drug development, disease areas, endpoints, and study designs.
What to Expect:
* A friendly working environment supporting personal and professional growth
* Supportive management fostering development
* A unique CRO approach to staff and project management
* Opportunities to own your role and develop skills
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