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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Hemel Hempstead
Client: Veramed
Location: Hemel Hempstead, 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, support, and training for career growth.
We have an exciting opportunity for a Principal level Statistical Programmer 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 supervise staff or projects.
Key Responsibilities
The following tasks outline the scope of the position, which may vary based on business needs:
Technical
* Review clinical trial documents (protocols, SAPs, CRFs, CRSs)
* Author, review, and approve study TFL shells and dataset specifications
* Develop, validate, and document SAS programs, ensuring good programming practices
* Identify data issues and outliers
* Complete and review CDISC Validation reports
* Resolve or escalate data and standards issues
* Stay informed of emerging standards and their impact
* Maintain SAS proficiency and awareness of developments
* Keep study master files audit-ready
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff for excellence
* Recruit, onboard, and integrate new team members
* Provide technical leadership and coaching
Project Management
* Manage client projects and portfolios
* Maintain project plans
* Manage resources, scope, and risks proactively
* Deliver projects within budget
* Manage client expectations and resolve issues
General
* Lead study, project, and team meetings
* Present updates internally and to clients
* Share 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 relevant industry experience
* At least 6 years of relevant 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 in staff and project management
* Opportunities to own your role and develop skills
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