Posted in Other about 2 hours ago.
Location: Nashville, Tennessee
The post-doctoral research associate should have a prior experience with multi-tasking skills in working with clinical/medical/dental research. He / She will directly assist clinical faculty on oral specimen collection & processing including blood, record keeping, data analysis, assist in IRB protocols. He / She is responsible in establishing clinical standard operating procedures (SOP), collecting and storing oral (Saliva, throat wash, dental plaque, oral swabs etc) and blood specimens as part of research project(s) by following study protocols. This person must have adequate wet lab (ELISA's, Protein, RNA experiments; cellular/molecular) research experience, including microbiome and cytokine analysis in all kinds of specimens. In addition, this person will assist with preparing IRB protocols, scheduling scientific meetings between collaborators, and transfer the specimens to other laboratories. The Research Associate is responsible in saving all patient information (all IRB documents, SOP) & research data in lock and key and help the faculty in working with IRB during entire research period.
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