Job Description
Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and offering 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 can offer home and/or office working, training, support, and a competitive package.
The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory roles (e.g., line management and/or project management).
Key Responsibilities
The tasks outlined below define the scope of the position, which 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 awareness of emerging standards and their impact on ongoing and future trials
* Maintain proficiency in SAS and stay updated on developments
* Maintain study master file documents and other audit-ready documents
People Management
* Line management of statisticians, programmers, and other technical staff, responsible for overall performance
* Provide coaching, mentoring, and career development for staff
* Interview, onboard, and integrate new team members effectively
* Provide technical leadership and coaching in programming
Project Management
* Oversee key client projects and portfolios, acting as Veramed 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 internal and client study, project, and cross-functional team meetings effectively
* Present study updates internally and at client meetings
* Share scientific, technical, and practical knowledge within the team and with colleagues
* Ensure compliance with internal and client policies, procedures, and training
* Build collaborative relationships with internal and client team members
* Share learnings across projects or studies
* Develop and deliver internal technical training where appropriate
* Lead process improvement initiatives
Minimum Qualifications
* BSc, MSc, or PhD in a numerical discipline or relevant industry experience
* At least 6 years of relevant industry experience
Additional Requirements
* Understanding of the clinical drug development process, relevant disease areas, endpoints, and study designs
What to Expect
* A warm, friendly working environment to thrive both personally and professionally
* A supportive management policy aiding your development and career progression
* A unique CRO approach to managing staff, projects, and industry relationships
* The opportunity to own your role and develop your skills and experience
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