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CPL Resources
83 Merrion Square, Dublin 2, Dublin
Phone: 01 614 6000

Web: http://www.cpljobs.ie/ E-mail: info@cpl.ie

Statistician


LD6577

clinical statistics clinical research Jobs clinical trials SAS statistician

Dublin South Leinster UK

Negotiable

1 - 2 Years

Permanent Full-time

See Description

01 278 4703

Linda.Dunne@thornshaw.com

Our client, are currently looking to recruit a Statistician. This role can be based in Dublin or in Marlow, UK.

Role Responsibility
Under the supervision of senior biostatisticians, this position is responsible for statistical aspects of clinical and preclinical research projects.  Project responsibilities include case report form development, statistical analysis and interpretation of data, and reporting of results.
 
In addition, your tasks will include:
·Assists senior biostatisticians in providing statistical support for clinical studies, including study design, sample size calculations, patient randomization, statistical analyses, interpretation of data, and reporting of results.
·Assists senior biostatisticians in statistical aspects of case report form design.
· Assists senior biostatisticians in 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 company standard operating procedures (SOPs) and study specific procedures (SSPs).
·Writes data quality control specifications for projects as needed.
· Understands and uses relevant computer languages and software packages. Writes programs to select, retrieve, manipulate, edit, and analyze data.
Monitors and verifies statistical analysis programs written by statistical programmers.
·Conducts statistical analyses and interprets results of these analyses.
·Prepares statistical summary reports under the supervision of senior biostatisticians.
· Writes the statistical methods sections of integrated study reports.  Reviews 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.

Experience and Qualification
M.S. degree in statistics, biostatistics, or related field.
Excellent verbal and written communication skills are required.
Knowledge in applied parametric and nonparametric statistics and strong SAS programming skills are a must.
Should be able to translate clients’ needs into statistical practice and educate clients in the use of statistics.

For more information on these job opportunities please email you CV to ldunne@thornshaw.com or call Linda on 01-2784671 for further information. For a list of all our jobs please log on to our website www.thornshaw.com
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Keywords: Jobs, clinical trials, clinical research, clinical, statistics, statistician, SAS


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