Clinical Statistician

Job type:
on-site
Start:
07/2013
Duration:
12 Months
From:
Real Staffing
Place:
Des Plaines
Date:
07/16/2013
Country:
flag_no USA
project ID:
567472

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This project is archived and not active any more.
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Provide statistical expertise for study case report for design, data base structure, analysis plan, and review of the study protocols and reports. Perform data analysis and provide statistical support including collaboration with medical groups to complete joint scientific reports and FDA overviews, including review of such reports to ensure accuracy and clarity. Must have clinical research experience.

Responsible for all statistical deliverables within assigned projects.

* Perform SAS programming to generate statistical analyses of data with appropriate guidance.

* Prepare Statistical Analysis Plans with appropriate guidance from senior staff.

* Collaborate with clinical team and data management/vendor on case report form design, query design and data cleaning.

* Prepare statistical sections of protocols, including sample size calculations.

* SAS programming and related activities for the presentation and analysis of clinical trial data.

* Carry out all activities according to appropriate SOPs.

Qualifications: MS or Ph. D degree in statistics or biostatistics. 1-3 Years Experience Level. Prior IVD or clinical research experience is preferred. Good SAS skills needed. Strong communication skill desired. The manager would like to see resumes with some industry experience.

This position requires a Masters degree or Ph.D

To find out more about Real please visit www.realstaffing.com