Statistician

Responsibilities-

-Represent Statistics on project teams, and serve as statistical contact with clients.
-Assist in establishing statistical processes and other administrative duties.
-Prepare or provide input into statistical sections of protocols, including sample size calculations
-Develop randomization specifications and verify randomization codes
-Conduct all statistical analyses in support of clinical research studies.
-Provide specifications for structure, content and algorithms for safety and efficacy analysis datasets to programmers.
-Perform quality control of safety and efficacy analysis datasets.
-Write statistical reports and statistical section of the clinical study report (CSR).
-Participate in dose escalation/safety review committees.
-Prepare detailed statistical analysis plans, including shells for tables, listings, and figures (TLFs).
-Actively provide feedback to Clinical Data Management on case report form (CRF) design, data management plan, and edit specifications.
-Handle miscellaneous tasks as assigned by management.
-Masters degree/Ph.D. in Statistics/Biostatistics or equivalent.
-4-6 years for M.S. and 3-5 years for Ph.D. in clinical data experience.
-Experience in endocrinology, specifically diabetes highly preferred.
-Experience analyzing glucose clamp data desired.

This is an excellent opportunity to gain experience working with an emerging leader in Clinical Research.
To find out more about Real please visit www.realstaffing.com