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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Oxford district
Client: Veramed
Location: Oxford district, United Kingdom
Job Category: Other
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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 level 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 roles such as line or project management.
Key Responsibilities
The tasks below outline the scope of the position, which may vary based on business needs.
Technical
* Review clinical trial documents including protocols, SAPs, CRFs, and CSRs.
* Author, review, and approve study TFL shells and dataset specifications.
* Develop, validate, and document SAS programs, ensuring good programming practices.
* Identify data issues and outliers.
* Review and approve CDISC Validation reports.
* Resolve or escalate data and standards issues.
* Stay updated on emerging standards and their impact.
* Maintain proficiency in SAS and stay aware of developments.
* Keep study master files and audit-ready documents.
People Management
* Line management of statisticians, programmers, and technical staff.
* Coach and mentor staff, support career development, and ensure training.
* Interview, onboard, and integrate new staff.
* Provide technical leadership and coaching.
Project Management
* Oversee client projects and portfolios, acting as Project Manager.
* Maintain project plans and proactively 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 scientific and technical knowledge.
* 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-door management policy supporting career development.
* A unique CRO with innovative staff and project management approaches.
* Opportunities to own your role and develop skills and experience.
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