Senior Biostatistician

The Senior Biostatistician will design and execute statistical analysis in support of clinical projects; prepare tables, listings, and figures presenting clinical data summaries for inclusion in reports; and provide statistical support to Company staff and clients.  Key responsibilities include:  reviewing and advising Company staff and clients with respect to clinical protocol design and planning of statistical procedures; developing and writing Statistical Analysis Plans for clinical trials; designing tables, listings and figures for statistical reporting; developing, testing, maintaining, and archiving SAS program code to perform statistical analysis and generate statistical reports of clinical data; and performing statistical QC review of source code and output developed by other staff biostatisticians for statistical reports.  The successful candidate will also perform statistical review of clinical data and communicate data issues to data management and clinical staff; review and advise with respect to data collection devices, database structures, data review procedures, and data management plans for clinical trials; design and prepare randomization schedules for clinical trials; provide quality improvement and efficiency to department processes and SOPs; and act as a resource for industry knowledge and technical knowledge. A MS or PhD and 3 years of clinical biostatistics experience in the pharmaceutical industry, including familiarity with clinical research reports and protocols are required. Excellent oral and written communication skills as well as knowledge of and experience with Contract Research Organization (CRO) processes are also required.

Please refer to job code LF6625 when responding to this ad.

Category:	Biotech/Pharmaceutical
	> Biostatistics
Location:	Lodi, NJ
County:	Bergen County
ZIP Code:	07644
Pay Rate:	Open
Job Terms:	full time
Company:	The Cambridge Group Ltd.
Phone:	E-mail or fax only
Fax:	203-226-3856