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Principal Statistical Programmer - Remote, Office or Hybrid - UK, York
Client: Veramed
Location:
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 role 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, with potential supervisory responsibilities.
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 and validate SAS programs for datasets, TFLs, and macros, following good programming practices
* Identify data issues and outliers
* Complete and review CDISC validation reports
* Address data and standards issues appropriately
* Stay updated on emerging standards and their impact
* Maintain SAS proficiency and awareness of developments
* Keep study documentation audit-ready
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff, supporting career development and training
* Hire, onboard, and integrate new team members
* Provide technical leadership and coaching
Project Management
* Manage client projects and portfolios
* Maintain project plans
* Manage resources, scope changes, and risks proactively
* Ensure projects are delivered within budget
* Manage client expectations and resolve issues
General
* Lead internal and client meetings effectively
* Present study updates internally and externally
* Share technical and scientific knowledge
* Ensure compliance with policies and procedures
* Build collaborative relationships
* Share learnings across projects
* Develop and deliver internal training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or relevant industry experience
* Minimum 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
* Open-door management fostering development
* A unique CRO approach to staff, projects, and relationships
* Opportunities to own your role and develop skills
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