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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Bournemouth
Client: Veramed
Location: Bournemouth, 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 a supportive working environment and career development opportunities.
We are seeking a Principal Statistical Programmer for a permanent position in the UK, offering home and/or office work, training, and a competitive package.
The role involves providing programming support across various projects and therapeutic areas, with potential supervisory responsibilities.
Key Responsibilities
The following tasks outline the scope of the role, which may vary based on business needs.
Technical
* Review clinical trial documents such as protocols, SAPs, CRFs, CSRs
* Author, review, and approve study TFL shells and dataset specifications
* Develop, validate, and document SAS programs following good programming practices
* Identify data issues and outliers
* Review CDISC Validation reports
* Resolve data and standards issues or escalate as needed
* Stay informed on emerging standards and their impact on trials
* Maintain SAS proficiency and stay updated on developments
* Ensure study documents are audit-ready
People Management
* Manage statisticians, programmers, and technical staff, overseeing performance
* Coach and mentor team members 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 and with colleagues
* Ensure compliance with policies and procedures
* Build collaborative relationships with internal and external teams
* 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-door management policy for development and career progression
* A unique CRO with innovative staff and project management approaches
* Opportunities to own your role and develop skills
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