Social network you want to login/join with:
Principal Statistical Programmer - Remote, Office or Hybrid - UK, Newport
Client: Veramed
Location: Newport, 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 industry-leading working environment supporting 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 such as line or project management.
Key Responsibilities
The following tasks outline the scope of the role, which may vary based on business needs:
Technical
* Review clinical trial documents like 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
* Identify data issues and outliers
* Review CDISC Validation tool reports
* Address data and standards issues appropriately
* Stay updated on emerging standards and their impact
* Maintain SAS proficiency and stay informed about developments
* Ensure audit readiness of study documents
People Management
* Manage statisticians, programmers, and technical staff
* Coach and mentor staff, supporting career development
* Hire and onboard 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 study, project, and team meetings
* Present updates internally and to clients
* Share technical knowledge within the team
* Ensure compliance with policies and procedures
* Build collaborative relationships
* Share learnings across projects
* Develop 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 with innovative management and relationship-building
* Opportunities to own your role and develop skills
#J-18808-Ljbffr