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Principal Statistical Programmer - Remote, Office or Hybrid - UK, south west london
Client: Veramed
Location: south west london, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Views: 3
Posted: 26.06.2025
Expiry Date: 10.08.2025
Job Description:
Veramed prides itself on providing high-quality statistics and programming consultancy, and offering an industry-leading working environment with support and training for career growth.
We have an exciting opportunity for a Principal Statistical Programmer in the UK. We offer 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 perform supervisory roles, such as line or project management.
Key Responsibilities
The following outlines the scope of the position, which may vary based on business needs:
Technical
* Review clinical trial documents (protocols, SAPs, CRFs, CRSs)
* Author, review, and approve study TFL shells and dataset specifications
* Develop, validate, and document SAS programs, ensuring good programming practices
* Identify data issues and outliers
* Review CDISC Validation reports
* Resolve or escalate data and standards issues
* Stay updated on emerging standards and their impact
* Maintain proficiency in SAS and awareness of developments
* Ensure audit readiness of study documents
People Management
* Line management of statisticians, programmers, and technical staff
* Coach and mentor staff for excellence
* Manage employee career development and training
* Onboard new staff members effectively
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios
* Serve as Veramed Project Manager on client accounts
* Maintain project plans
* Manage resources, scope, and risks proactively
* Ensure project delivery within budget
* Manage client expectations and resolve issues
General
* Lead study, project, and cross-functional team meetings
* Present updates internally and to clients
* Share scientific, technical, and practical knowledge
* Ensure compliance with policies and procedures
* Build collaborative relationships
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or relevant experience
* At least 6 years of industry experience
Other Information/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 policy for development
* A unique CRO culture focusing on staff, projects, and relationships
* Opportunities for role ownership and skill development
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