Act as primary study coordinator for multiple research studies. Screen, recruit, and get consent from research participants following study protocols and Good Clinical Practice guidelines. Schedule and conduct research visit with participants. Collect specimens and monitor participants. Complete study activities outlined in study protocols. Report problems or protocol deviations to the Principal Investigator and senior research personnel. Create and update standard operating procedures, manage study data, and generate reports. Assist with creating electronic data capture systems using Redcap and Qualtrics. Assist with creation of posters, manuscripts, and presentations for scientific meetings and/or grant submissions, including conducting literature reviews, drafting content for manuscripts and presentations, report generation, and creating graphs and diagrams. Manage regulatory and reporting documentation for assigned studies.
The employee will recruit, screen, and consent research participants; schedule and conduct research visits with participants remotely and in-person; collect specimens and monitor participants according to the IRB protocols established; and input data into REDCap (data capture system). The employee will create and update standard operating procedures, manage study data, and generate reports. They will also assist with the creation of posters, manuscripts, and presentations for scientific meetings and/or grant submissions and be responsible for preparing IRB applications, amendments, scheduled continuing reviews, and adverse event reports. Remote work-from-home up to 100% anywhere in United States permitted.
