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Principal Statistical Programmer - Remote, Office or Hybrid - UK, High Wycombe
Client: Veramed
Location: High Wycombe, 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 excellent working environment supporting career growth.
We are seeking a Principal Statistical Programmer for a permanent position in the UK, offering home/office work options, training, and a competitive package.
The role involves providing programming support across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also have supervisory responsibilities, including line management and project oversight.
Key Responsibilities
The following outlines the scope of the role, which 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
* Review and approve CDISC Validation reports
* Resolve data and standards issues or escalate as needed
* Stay informed about emerging standards and their impact on trials
* Maintain SAS proficiency and stay updated on developments
* Keep study master files and audit-ready documents
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff to achieve excellence
* Handle onboarding and integration of new team members
* Provide technical leadership and coaching
Project Management
* Oversee client projects and portfolios, acting as Project Manager
* Maintain project plans and manage resources, scope, and risks
* Ensure projects are delivered within budget
* Manage client expectations and resolve issues
General
* Lead internal and client meetings effectively
* Present study updates and share knowledge
* Ensure compliance with policies and procedures
* Build collaborative relationships within teams
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications include a BSc, MSc, or PhD in a numerical discipline or equivalent experience, with at least 6 years of 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 approach to staff and project management
* Opportunities for role ownership and skill development
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