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Über
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- 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. xcfaprz
- 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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Sprachkenntnisse
- English
Hinweis für Nutzer
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