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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Basildon
Client: Veramed
Location: Basildon, United Kingdom
Job Category: Other
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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 role in the UK, offering flexible work arrangements, training, and a competitive package.
The role involves providing programming support across various projects and therapeutic areas, with potential supervisory responsibilities such as line and project management.
Key Responsibilities
The tasks below outline the role's scope, 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
* Address data and standards issues appropriately
* Stay informed of emerging standards and their impact
* Maintain proficiency in SAS and stay updated on developments
* Ensure audit readiness of study documentation
People Management
* Manage statisticians, programmers, and technical staff, overseeing their performance
* Mentor and coach staff to achieve excellence
* Handle onboarding and integration of new team members
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios
* Manage project plans, resources, scope, and risks
* Ensure projects are delivered within budget
* Manage client expectations and resolve issues
General
* Lead team meetings and present updates
* Share knowledge within the team
* Ensure compliance with policies and procedures
* Build collaborative relationships internally and with clients
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or equivalent experience
* Minimum 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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