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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Preston, Lancashire
Client:
Veramed
Location:
Preston, Lancashire, United Kingdom
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, offering 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 have supervisory responsibilities, including line and project management.
Key Responsibilities
Technical
* Review of clinical trial documents such as protocols, SAPs, CRFs, and CSRs
* Authoring, reviewing, and approving study TFL shells and dataset specifications
* Authoring, validating, and documenting SAS programs following good programming practices
* Identifying data issues and outliers
* Reviewing CDISC Validation reports
* Resolving data and standards issues or escalating as needed
* Staying updated on emerging standards and their impact on trials
* Maintaining SAS proficiency and awareness of developments
* Managing study documentation for audits
People Management
* Line management of statisticians, programmers, and technical staff
* Coaching and mentoring staff to achieve excellence
* Managing staff performance, training, and development
* Onboarding new staff members
* Providing technical leadership and coaching
Project Management
* Overseeing client projects and portfolios
* Managing project plans, resources, scope, and risks
* Ensuring projects are delivered within budget
* Managing client expectations and resolving issues
General
* Leading study, project, and team meetings
* Presenting updates to internal teams and clients
* Sharing technical knowledge within the team
* Ensuring compliance with policies and procedures
* Building collaborative relationships
* Sharing learnings across projects
* Developing internal technical training
Qualifications
BSc, MSc, or PhD in a numerical discipline or relevant industry experience; at least 6 years of relevant 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 culture emphasizing staff management, projects, and relationships
* Opportunities for role ownership and skill development
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