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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Derby
Client: Veramed
Location: Derby, 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 position offers flexible working arrangements, training, support, and a competitive package.
The role involves providing programming support across various projects, clients, and therapeutic areas, with potential supervisory responsibilities.
Key Responsibilities
The tasks below outline the scope; actual duties 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 following good programming practices
* Identify data issues and outliers
* Complete, review, and approve CDISC Validation reports
* Address data and standards issues appropriately
* Stay updated on emerging standards and their impact on trials
* Maintain proficiency in SAS and stay informed about developments
* Ensure study documentation is audit-ready
People Management
* Manage statisticians, programmers, and technical staff, overseeing 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
* Manage project plans, resources, scope, and risks
* Deliver projects 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
* Ensure compliance with policies and procedures
* Build collaborative relationships
* Share learnings across projects
* Provide internal technical 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 working environment
* Opportunities for professional development
* A unique CRO culture focused on staff management and relationship building
* Ownership of your role and skill development
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