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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Worcester
Client:
Veramed
Location:
Worcester, 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, 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 perform supervisory duties, including line and project management.
Key Responsibilities
The following tasks outline the role's scope, 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
* Identify data issues and outliers
* Review CDISC Validation tool reports
* Resolve data and standards issues or escalate as needed
* Stay informed on emerging standards and their impact
* Maintain proficiency in SAS and stay updated on developments
* Ensure audit readiness of study master files and related documents
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff to achieve excellence
* Handle hiring, onboarding, and training of new staff
* Provide technical leadership and coaching
Project Management
* Oversee client projects and portfolios
* Act as Project Manager on client accounts
* Maintain project plans and manage resources, scope, and risks
* Ensure project delivery within budget
* Manage client expectations and resolve issues
General
* Lead study, project, and team meetings
* Present updates internally and to clients
* Share scientific and technical knowledge
* Ensure compliance 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 relevant experience
* Minimum 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
* Management that fosters development and career growth
* A unique CRO approach to managing staff and projects
* Opportunities to own your role and develop skills
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