Social network you want to login/join with:
Principal Statistical Programmer - Remote, Office or Hybrid - UK, Cheltenham
Client: Veramed
Location: Cheltenham, UK
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 have an exciting opportunity for a Principal Statistical Programmer to join us on a permanent basis in the UK. We offer 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 such as line or project management.
Key Responsibilities
The following tasks 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
* Review and approve CDISC Validation reports
* Address data and standards issues appropriately
* Stay aware of emerging standards and their impact on trials
* Maintain proficiency in SAS and stay updated on developments
* Ensure study master files and audit-ready documents are maintained
People Management
* Line management of statisticians, programmers, and technical staff, overseeing performance
* Coach, mentor, and support staff career development and training
* Interview, onboard, and integrate new team members
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios, acting as Project Manager
* Maintain project plans and proactively manage resources, scope, and risks
* Ensure project delivery within budget
* Manage client expectations and resolve issues
General
* Lead internal and client meetings effectively
* Present study updates internally and externally
* Share knowledge within the team and with colleagues
* Ensure compliance with policies and procedures
* Build collaborative relationships with teams and clients
* Share learnings across projects
* Develop and deliver internal technical 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 for personal and professional growth
* Open management policy supporting career development
* A unique CRO approach to staff and project management
* Opportunities to own your role and develop skills
#J-18808-Ljbffr