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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Guildford
Client: Veramed
Location: Guildford, 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, and a competitive package.
The role involves providing programming support across various projects and therapeutic areas, with potential supervisory responsibilities such as line or project management.
Key Responsibilities:
* Review clinical trial documents including 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 updated on emerging standards and their impact on trials
* Maintain proficiency in SAS and stay informed on developments
* Ensure study documents are audit-ready
People Management:
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff to achieve excellence
* Handle recruitment, onboarding, and training of new staff
* Provide technical leadership and coaching
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 study, project, and team meetings effectively
* 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 and deliver technical training
Qualifications:
* BSc, MSc, or PhD in a relevant numerical discipline or equivalent 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 work environment
* Open-door management fostering development
* A unique CRO approach to managing staff and projects
* Opportunities for role ownership and skill development
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