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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Chelmsford
Client:
Veramed
Location:
UK, Chelmsford
Job Category:
Other
EU work permit required: Yes
Job Views: 9
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. The position offers flexible working arrangements, 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 management and project management.
Key Responsibilities
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 and escalate as needed
* Stay updated on emerging standards and their impact on trials
* Maintain proficiency in SAS and stay informed of 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 recruitment, onboarding, and training of new staff
* Provide technical leadership and coaching
Project Management
* Oversee client projects and portfolios, acting as Project Manager
* Maintain project plans and manage resources, scope, and risks
* Ensure projects are delivered within budget
* Manage client expectations and resolve issues
General
* Lead study, project, and team meetings effectively
* Present updates internally and to clients
* Share knowledge within the team
* Ensure compliance with policies and procedures
* Build collaborative relationships with team members
* Share learnings across projects
* Develop and deliver internal technical training
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or equivalent 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 fostering personal and professional growth
* Open-door management policy and career development tools
* A unique CRO culture emphasizing staff management, project handling, and industry relationships
* Opportunities to own your role and develop your skills
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