Job Description
Responsibilities include, but are not limited to:Scan documents into the electronic medical record.Obtain signatures for essential documents.Assist with managing collection of human subject trainings, CVs (signed/dated), medical licenses (signed/dated), CTEP registrations, MLs, and assist in organizing and maintaining paper and electronic regulatory binders.Assist with maintaining central files, data tracking systems, and ad hoc reports.Assist in the organization of supplies received for clinical trials.Assist with organizing clinical research data and data collection/entry to institutional systems (VELOS/Study Manager).Clinical trials kit preparation and breakdown.Electronic study binder creation and organization into shared Departmental Drive and into the electronic medical records system EPIC.Scheduling testing and appointments as directed.
Responsibilities + Skills
Obtain signatures for essential documents.Assist with managing collection of human subject trainings, CVs (signed/dated), medical licenses (signed/dated), CTEP registrations, MLs, and assist in organizing and maintaining paper and electronic regulatory binders.
Education
Assist with maintaining central files, data tracking systems, and ad hoc reports.Assist in the organization of supplies received for clinical trials.Assist with organizing clinical research data and data collection/entry to institutional systems (VELOS/Study Manager).
Experience
