Location: Chicago, ILJob Description:Develop study protocols, CRFs, and other study documents.Develop instructional regulatory body (IRB) protocols, amendments and other documents as well as respond to IRB stipulations and requirements. Collect, archive subjectsâ™ data. Assist in scientific data dissemination. Develop, write, edit, submit and publish scientific manuscripts and present scientific abstract at national and international conferences. Participate in local and national meetings related to multi center trials and participate in regular phone/skype meetings related to clinical research.Assist in developing and submitting regular progres