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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Coventry
Client: Veramed
Location: Coventry, 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 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, such as line management or project management.
Key Responsibilities
The following tasks outline the scope of the role. Tasks may vary based on current 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
* 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 proficiency in SAS and stay updated with developments
* Keep study documentation audit-ready
People Management
* Line manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff to achieve excellence
* Manage employee career development and training
* Onboard and integrate new staff members effectively
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios
* Act as Veramed Project Manager on client accounts
* Maintain project plans, 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 internally and externally
* Share scientific, technical, and practical knowledge
* Ensure compliance with policies, procedures, and training
* Build collaborative relationships with internal and client teams
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or relevant industry experience
* Minimum 6 years of relevant industry experience
Additional Requirements
* Understanding of clinical drug development, disease areas, endpoints, and study designs
What to Expect:
* A supportive and friendly work environment for personal and professional growth
* Open-door management policy to aid development
* A unique CRO approach to staff, projects, and industry relationships
* Opportunities to own your role and develop skills
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