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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Bristol Client: Veramed
Location: Bristol, 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, with potential supervisory responsibilities.
Key Responsibilities The following tasks outline the scope of the position, which may vary based on business needs:
Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs
Author, review, and approve study TFL shells and dataset specifications
Develop, validate, and document SAS programs for datasets, TFLs, and macros, adhering to good programming practices
Identify data issues and outliers
Review and approve CDISC Validation reports
Address data and standards issues appropriately
Stay updated on emerging standards and their impact on trials
Maintain proficiency in SAS and stay informed about developments
Ensure study documentation is audit-ready
People Management Line management of statisticians, programmers, and technical staff
Coach and mentor staff to achieve excellence
Oversee employee career development and training
Recruit and onboard new staff effectively
Provide technical leadership and coaching
Project Management Manage client projects and portfolios
Maintain project plans
Proactively manage resources, scope, and risks
Deliver projects 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
Share learnings across projects
Develop and deliver internal technical training
Qualifications include a BSc, MSc, or PhD in a numerical discipline (or equivalent experience), and 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 and friendly work environment
Open-door management policy for development
A unique CRO approach to staff and project management
Opportunities for role ownership and skill development
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