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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Wolverhampton
Client: Veramed
Location: Wolverhampton, UK
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 industry-leading working environment supporting career growth.
We are seeking a Principal Statistical Programmer for a permanent position in the UK, offering home and/or office work, 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 (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
* Complete, review, and approve CDISC Validation reports
* Resolve or escalate data and standards issues
* Stay informed on emerging standards and their impact on trials
* Maintain proficiency in SAS and stay updated with developments
* Maintain study master files and audit-ready documents
People Management
* Line management of statisticians, programmers, and technical staff
* Provide coaching, mentoring, and career development for staff
* Recruit, onboard, and integrate new team members
* Offer technical leadership and coaching
Project Management
* Oversee client projects and portfolios
* Manage project plans, resources, scope, and risks
* Ensure project delivery 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 and procedures
* Build collaborative relationships with internal and external 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 relevant industry experience
Additional Requirements
* Understanding of clinical drug development, disease areas, endpoints, and study designs
What to Expect:
* A supportive, friendly working environment for personal and professional growth
* Open-door management policy encouraging development
* A unique CRO with innovative staff and project management approaches
* Opportunities to own your role and develop skills
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