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RemX IT Staffing |
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Sr. BiostatisticianPosted: November 7, 2009
Our client has an immediate opening for a 3-6 month+ Contract BioStatistician who will be responsible for providing statistical support to assigned drug development programs, may include: writing statistical analysis plan, performing programming and planned statistical analyses and producing summary tables, listings and graphs, interpreting study results and writing statistical summary reports of study results.
Responsibilities: • Implement statistical analysis in conformance with defined programming processes and standard operating procedures; • Ensure that all programs, outputs and documentation are consistent with relevant ICH requirements and are conducted in compliance with relevant SOPs; • May develop statistical analysis plan • Perform programming and planned statistical analyses and produce summary tables, listings and graphs • May interpret study results and write statistical summary reports of study results
Requirements: • Masters degree in statistics or other relevant area with Ph.D. preferred • A minimum of 5 – 6 years experience in the pharmaceutical or biotechnology industries with broad knowledge of biostatistics, FDA/EMEA guidelines and drug development process, and SAS programming skill required. **This is 3-6+ month position. Hourly Rate is commensurate with experience. This client is not able to offer sponsorship at this time.**
For immediate consideration, please email a Word version of your current resume to Philadelphia@remxit.com and reference “161654-scd” in the subject line. Please refer to job code 161654-scd when responding to this ad.
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