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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Chesterfield
Client: Veramed
Location: Chesterfield, 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, and offering an industry-leading working environment with support and training for career growth.
We have an exciting opportunity for a Principal Statistical Programmer to join us on a permanent basis in the UK. We offer flexible working arrangements, training, support, and a competitive package.
The role involves providing programming support to the statistics and programming department across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory duties, such as line or project management.
Key Responsibilities
The tasks below outline the scope of the position, which may vary based on business needs.
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 for datasets, TFLs, and macros, following good programming practices
* Identify data issues and outliers
* Complete, review, and approve CDISC Validation reports
* Address data and standards issues appropriately
* Stay informed of emerging standards and their impact on trials
* 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 their performance
* Provide coaching, mentoring, and career development for team members
* Recruit, onboard, and integrate new staff
* Offer technical leadership and coaching
Project Management
* Oversee key client projects and portfolios, acting as Project Manager
* Maintain project plans, manage resources, scope, and risks
* 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 scientific, technical, and practical knowledge
* Ensure compliance with policies and procedures
* Build collaborative relationships within teams
* Share learnings across projects
* Develop and deliver internal 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, friendly working environment for personal and professional growth
* Open-door management policy for development and career progression
* A unique CRO experience focused on staff, project, and relationship management
* Opportunities to own your role and develop skills
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