Sort by
Refine Your Search
-
Listed
-
Field
-
. The successful candidate, under the Principal Investigator's supervision, will handle MRI and demographic data management, quality control, and pre-processing, manage MRI processing pipelines, and prepare IRB/CCI
-
and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical study standards and procedures
-
for studies. Prepares IRB and/or CCI documentation and submissions in conjunction with the Principal Investigator and /or other members of the research team. Conducts data collection activities and prepares
-
forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical study standards and
-
be carried out utilizing a range of laboratory equipment and will entail accurately documenting procedures undertaken, recording any data generated, and performing a variety of downstream data analysis
-
children newly diagnosed with T1D. The ideal candidate will have excellent organizational, communication, time management, and computer skills (Word, Excel, PowerPoint) and will have experience and/or
-
patients for research studies through personal interviews and written communications with patients/families. Provide detailed background information regarding studies to families, communicate all policies
-
toxic materials. Carries out all laboratory activities in compliance with applicable regulations and protocols. Conducts literature searches and reviews, compiling information for journals and suggesting