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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Southampton
Client: Veramed
Location: Southampton, 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, clients, and therapeutic areas, with potential supervisory responsibilities.
Key Responsibilities:
Technical:
* 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, ensuring good programming practices
* Identify data issues and outliers
* Review CDISC validation reports
* Resolve data and standards issues
* Stay updated on emerging standards and their impact
* Maintain SAS proficiency and awareness of developments
* Ensure audit-ready study documentation
People Management:
* Line management of statisticians, programmers, and technical staff
* Coach and mentor staff for excellence
* Manage employee development and training
* Recruit and onboard new staff
* Provide technical leadership and coaching
Project Management:
* Oversee key client projects and portfolios
* Manage project plans, resources, scope, and risks
* Ensure projects are delivered within budget
* Manage client expectations and resolve issues
General:
* Lead study, project, and team meetings
* Present updates internally and to clients
* Share knowledge and develop internal training
* Comply with policies and procedures
* Build collaborative relationships
* Share learnings across projects
* Develop internal technical training
Qualifications:
* BSc, MSc, or PhD in a 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, friendly working environment
* Open-door management policy for development
* A unique CRO with innovative management and relationship-building
* Opportunities to own your role and develop skills
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