Senior Biostatistician II
About the role
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- Provides statistical support for clinical studies, including study design, sample size calculations, patient randomization, statistical analyses, interpretation of data, and reporting of results.
- Writing statistical analysis plans, including the definition of derived data sets, and the design of statistical tables, figures, and data listings for clinical summary reports.
- Carries out project related work in accordance with ICON standard operating procedures (SOPs) and study specific procedures (SSPs).
- Understands and uses relevant computer languages and software packages (e.g. SAS).
- Writes programs to select, retrieve, manipulate, edit, and analyse data.
- Monitors and verifies statistical analysis programs written by statistical programmers.
- Conducts selected statistical analyses and interprets results of these analyses.
- Writes the statistical methods sections of integrated study reports. Reviews and approves draft integrated study reports.
- Documents and archives analysis and programming work to ensure a complete audit trail. Participates in the setting of project document standards.
- Creates and maintains biostatistics files for each assigned project.
- Manages statistics and programming projects to high quality, within budget, and on-time completion.
- Establishes and maintains effective working relationships with clients and ICON project team members, including data management personnel, statistical programmers, and clinical research personnel.
- Participates in presentations at client and investigator meetings.
- Assists in the preparation of biostatistics input to ICON research proposals.
- Researches and applies new statistical procedures as needed.
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