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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Maidstone
Client: Veramed
Location: Maidstone, 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 excellent 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. The Senior or Principal Programmer may also have supervisory responsibilities, including line and project management.
Key Responsibilities
The tasks below outline the scope of the role, which may vary based on business needs.
Technical
* Review clinical trial documents such as 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 of emerging standards and their impact on trials
* Maintain SAS proficiency and awareness of developments
* Keep study master files and audit-ready documentation
People Management
* Manage statisticians, programmers, and technical staff; responsible for their performance
* Coach and mentor staff for excellence; oversee career development and training
* Recruit, onboard, and integrate new team members
* Provide technical leadership and coaching in programming
Project Management
* Oversee client projects and portfolios, acting as Project Manager
* Maintain project plans
* Manage resources, scope, risks, and budgets
* Manage client expectations and resolve issues
General
* Lead internal and client meetings effectively
* Present study updates
* Share knowledge within and outside the team
* Ensure compliance with policies and procedures
* Build collaborative relationships with teams
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or relevant industry experience
* 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 working environment
* Opportunities for professional development
* A unique CRO with innovative management and relationship-building
* Role ownership and skill development opportunities
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