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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Peterborough
Client: Veramed
Location: Peterborough, 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 fostering an industry-leading working environment with support and training for career growth.
We are seeking a Principal Statistical Programmer for a permanent role in the UK, offering home and/or office working, 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 following outlines the scope of the position, which may vary based on business needs.
Technical
* Review clinical trial documents such as 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
* Complete, review, and approve CDISC Validation reports
* Address data and standards issues appropriately
* Stay informed about emerging standards and their impact on trials
* Maintain proficiency in SAS and stay updated on developments
* Ensure study master files and other audit-ready documents are maintained
People Management
* Manage statisticians, programmers, and technical staff, overseeing their 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 as Project Manager
* Maintain project plans and proactively manage resources, scope, and risks
* Deliver projects within budget
* Manage client expectations and resolve issues
General
* Lead study, project, and team meetings effectively
* Present updates to internal teams and clients
* Share knowledge within the team and externally
* Ensure compliance with policies and procedures
* Build collaborative relationships with internal and client teams
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or equivalent 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 working environment
* Open-door management policy for career development
* A unique CRO approach to staff and project management
* Opportunities for role ownership and skill development
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