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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Watford, Hertfordshire
Client: Veramed
Location: Watford, Hertfordshire, 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, and offering an industry-leading working environment with support and training for career growth.
We have an exciting opportunity for a Principal level Statistical Programmer to join us on a permanent basis 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 management and project management.
Key Responsibilities
The tasks below outline the scope of the position, which may vary based on current business needs.
Technical
* Review of clinical trial documents including protocols, SAPs, CRFs, CSRs
* Author, review, and approve study TFL shells and dataset specifications
* Author, 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
* Identify and resolve or escalate data and standards issues
* Stay aware of emerging standards and their impact on trials
* Maintain proficiency in SAS and stay updated on developments
* Maintain study master file documents to be audit-ready
People Management
* Line management of statisticians, programmers, and technical staff
* Provide coaching, mentoring, and career development for staff
* Interview, onboard, and integrate new staff members
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios
* Act as Veramed Project Manager on client accounts
* Maintain project plans, manage resources, scope, risks, and budgets
* Manage client expectations and resolve issues
General
* Lead internal and client meetings effectively
* Present study updates internally and externally
* Share scientific, technical, and practical knowledge
* Ensure compliance with policies and procedures
* Build collaborative relationships with teams and clients
* 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 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 for development
* A unique CRO experience with innovative staff and project management
* Opportunities to own your role and develop skills
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