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Principal Statistical Programmer - Remote, Office or Hybrid - UK, West Midlands
Client: Veramed
Location: UK, West Midlands
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 position in the UK, offering remote and/or office work, training, support, and a competitive package.
The role involves providing programming support across various projects, clients, and therapeutic areas, with potential supervisory responsibilities such as 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 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, 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 awareness of developments
* Ensure audit readiness of study documentation
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff to achieve excellence
* Handle recruitment, onboarding, and training of new staff
* Provide technical leadership and coaching
Project Management
* Oversee client projects and portfolios
* Act as Project Manager for 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 effectively
* Present updates to internal and client teams
* Share scientific and technical knowledge
* Ensure compliance with policies and procedures
* Foster collaborative relationships
* Share learnings across projects
* Develop internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or equivalent industry experience
* Minimum 6 years relevant industry experience
Additional Requirements
* Understanding of clinical drug development, disease areas, endpoints, and study designs
What to Expect:
* A supportive and friendly working environment
* Open-door management fostering development
* A unique CRO approach to staff, projects, and relationships
* Opportunities for role ownership and skill development
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