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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Leigh, Greater Manchester
Client: Veramed
Location: 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 excellent working environment supporting career growth.
We are seeking a Principal Statistical Programmer for a permanent role in the UK. The role offers flexible working options, 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 have supervisory responsibilities, including line and project management.
Key Responsibilities
Technical
* Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs
* Author, review, and approve study TFL shells and dataset specifications
* Develop and validate SAS programs, ensuring good programming practices
* Identify data issues and outliers
* Review CDISC validation reports
* Resolve data and standards issues or escalate as needed
* Stay informed about emerging standards and their impact on trials
* Maintain SAS proficiency and stay updated on developments
* Maintain study documentation for audits
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor staff for excellence and career development
* Recruit, onboard, and integrate new team members
* Provide technical leadership and coaching
Project Management
* Oversee key client projects and portfolios
* Serve as Veramed Project Manager for client accounts
* 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 and technical knowledge
* Ensure compliance with policies and procedures
* Build collaborative relationships
* 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 industry experience
Additional Requirements
* Understanding of clinical drug development, disease areas, endpoints, and study designs
What to Expect:
* A supportive and friendly working environment
* Open-door management policy for development
* A unique CRO with innovative staff and project management
* Opportunities to own and develop your role
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