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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Aberdeen
Client: Veramed
Location: UK, Aberdeen
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 that supports career growth.
We are seeking a Principal Statistical Programmer for a permanent position in the UK. We offer flexible working arrangements, 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
Technical
* Review clinical trial documents like protocols, SAPs, CRFs, CSRs
* Author, review, and approve study TFL shells and dataset specifications
* Develop and validate SAS programs for datasets, TFLs, and macros following good programming practices
* Identify data issues and outliers
* Review 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
* Keep study master files and audit-ready documentation
People Management
* Line management of statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff to achieve excellence
* Manage staff recruitment, onboarding, and training
* Provide technical leadership and coaching
Project Management
* Manage client projects and portfolios
* Maintain project plans
* Manage resources, scope, risks, and budgets
* Handle client expectations and resolve issues
General
* Lead internal and client meetings effectively
* Present updates internally and externally
* Share knowledge and develop internal training
* Ensure compliance with policies and procedures
* Build collaborative relationships
* Share learnings across projects
* Develop 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 and friendly working environment
* Management that supports your development
* A unique CRO with innovative management and relationship-building
* Opportunities to own your role and develop skills
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