Social network you want to login/join with:
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
#J-18808-Ljbffr