Main Function(s)
Third level degree in Statistics / Biomedical/Computer Science or related discipline.
Experience in SAS or equivalent programming language (eg: R, SPSS).
Excellent organisational, communication and time management skills.
Excellent attention to detail.
Ability to work autonomously as well as work in a team-based environment.
Oncology background/experience an advantage.
Proficiency in all Microsoft Office Tools and general computer literacy.
Primary Responsibilities
Work with Group Statistician in providing statistical support to Cancer Trials Ireland investigators regarding study design, endpoint selection and sample size calculation.
Provide statistical input to Case Report Form (CRF) and database design, also data.
Create, validate, execute, and generate statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables, figures) as planned in the Statistical Analysis Plan.
Writing, documenting, and performing quality control review of SAS programs.
Program, test and document specific listings and reports (e.g. Safety Monitory Committee reports, Data Safety Monitoring Board (DSMB) reports and End of Study Reports).
Develop tables, graphs for scientific publications as directed by Group Statistician.
Support Data Management activities including data review activity before database lock.
Provide technical advice and programming solutions for clinical projects.
Creation and review of technical specifications and applicable Standard Operating Procedures (SOP) / Study-specific procedures (SSP) / Work instructions.
Create and maintain study files and other appropriate study documentation.
Collaborate with team members to plan and deliver on Study Deliverables.
Adhere to all related procedures and regulations, e.g. Study Guidelines, SOPs, ICH GCP, etc.
Perform other tasks as specified by Head of Biometrics/Group Statistician.
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