Job Description
Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and offering its employees an industry-leading working environment with support and training for 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 and support, and a competitive package.
The purpose of the role is to provide programming support to the statistics and programming department across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory roles, such as line management and/or project management.
Key Responsibilities
The tasks listed below outline the scope of the position. The application of these tasks may vary based on current business needs.
Technical
Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
Author, review, and approve study TFL shells and dataset specifications
Author, validate, and document SAS programs for datasets, TFLs, and macros, applying good programming practices
Identify data issues and outliers
Complete, review, and approve CDISC Validation tool reports
Identify data and standards issues and resolve or escalate as appropriate
Maintain proficiency in SAS and awareness of developments
Maintain study master file documents and other audit-ready documents
People Management
Line management of statisticians, programmers, and other technical staff, accountable for overall performance
Provide coaching, mentoring, and career development for staff
Interview, onboard, and integrate new staff members
Provide programming technical leadership and coaching
Project Management
Oversee client projects and portfolios, including managing scope, resources, and risks
Maintain project plans and deliver projects within budget
Manage client expectations and resolve issues
General
Lead internal and client meetings effectively
Present study updates to internal teams and clients
Share scientific, technical, and practical knowledge within the team
Ensure compliance with policies, procedures, and training
Build collaborative relationships with internal and client teams
Share learnings across projects
Develop and deliver internal technical training
Lead process improvement initiatives
Minimum Qualification Requirements
BSc, MSc, or PhD in a numerical discipline or relevant industry experience
At least 6 years of relevant industry experience
Other Information/Additional Requirements
Understanding of clinical drug development, disease areas, endpoints, and study designs
What to Expect:
A supportive and friendly working environment for personal and professional growth
An open-door management policy to aid your development
A unique CRO that values staff, projects, and industry relationships
The opportunity to own your role and develop your skills and experience
#J-18808-Ljbffr