Primary responsibilities for these roles include providing
extensive biostatistical support in the planning, analysis, and
preparation of reports for clinical studies and registering drugs
in the US and internationally. Selected candidates will also
participate in the design and conduct of clinical studies and
evaluations and interpret and prepare study results for internal
reports and submissions to the FDA and other agencies. Other
duties include developing statistical programs, performing
analysis, preparing data displays and verifying data validity.
Experience must include consulting with research personnel,
including clinical researchers, and authorship on formal
reports and regulatory submissions. Must have demonstrated
knowledge of major statistical software packages (SAS and
Splus) and the ability to integrate statistical and biomedical
concepts. Familiarity with ICH guidelines and FDA
requirements is also required. Must have industry experience.
Geographic Location of Position: US-CT, NJ
Contact: Carol Andrews -
DMC.
Voice: 732-316-0169 ext.230 /
Fax: 609-584-9575 /
Email: 915814@candseek2.com.
