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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Gloucester
Client:
Veramed
Location:
Gloucester, 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, support, and training for career growth.
We are seeking a Principal Statistical Programmer for a permanent role in the UK. The role offers home and/or office working, training, support, and a competitive package.
The main purpose is to support the statistics and programming department across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also have supervisory responsibilities, including line management and project oversight.
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, and 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.
* Complete, review, and approve CDISC Validation reports.
* Address data and standards issues appropriately.
* Stay informed about emerging standards and their impact on trials.
* Maintain proficiency in SAS and stay updated on developments.
* Ensure study master files and audit-ready documentation are maintained.
People Management
* Manage statisticians, programmers, and technical staff, overseeing their performance.
* Coach and mentor staff to achieve excellence.
* Handle hiring, onboarding, and integration of new team members.
* Provide technical leadership and coaching.
Project Management
* Oversee key client projects and portfolios.
* Serve as Project Manager on client accounts.
* Maintain project plans and proactively 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 within the team.
* 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 include a BSc, MSc, or PhD in a numerical discipline (or equivalent industry experience) and a minimum of 6 years of relevant experience.
Additional Requirements
Understanding of clinical drug development, relevant disease areas, endpoints, and study designs.
What to Expect:
* A supportive and friendly working environment.
* Open-door management policy for development and career progression.
* A unique CRO approach to staff and project management.
* Opportunities for role ownership and skill development.
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