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Principal Statistical Programmer - Remote, Office or Hybrid - UK, Stevenage
Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working environment that supports 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, 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 take on supervisory responsibilities such as line management and project management.
Key Responsibilities
The scope of tasks includes:
* Review of clinical trial documents including protocols, SAPs, CRFs, CSRs
* Authoring, reviewing, and approving study TFL shells and dataset specifications
* Authoring, validating, and documenting SAS programs for datasets, TFLs, and macros, following good programming practices
* Identifying data issues and outliers
* Completing, reviewing, and approving CDISC Validation reports
* Addressing data and standards issues appropriately
* Maintaining proficiency in SAS and awareness of industry developments
* Ensuring audit readiness of study master files and related documents
People Management
Line management of statisticians, programmers, and technical staff, overseeing their performance, coaching, mentoring, and career development. Responsible for onboarding new staff and providing technical leadership.
Project Management
Managing client projects including planning, resource management, scope, risks, and budget. Ensuring effective communication and issue resolution.
General
Leading team meetings, presenting updates, sharing knowledge, ensuring compliance, building collaborative relationships, and developing internal training.
Qualifications
BSc, MSc, or PhD in a numerical discipline or relevant industry experience, with 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 work environment that fosters personal and professional growth.
* Open management policy and career development tools.
* A unique CRO approach to staff, projects, and industry relationships.
* Opportunities to own your role and develop skills.
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