Human Subject Research Spec I

Coordinates the administrative activities associated with conducting multi-site, decentralized or other research studies. May assist Principal Investigator in conducting clinical studies, and in presenting study research results. Interacts with study sponsor and partners on research projects.

Responsibilities

Coordinates the administrative activities associated with conducting multi-site, decentralized or other research studies; May assist Principal Investigator in conducting clinical studies, and in presenting study research results; Interacts with study sponsor and partners on research projects; Coordinates administrative activities necessary for clinical studies such as maintaining protocol and PI brochures, preparing materials for study visits, drafting and maintaining informed consent documents, and preparing study materials; Trains staff on details of protocol including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form completion, and adverse event reporting; Develops recruitment strategies and targets; Recruits and consents participants for research studies; Conducts remote and/or in-person assessments of research participants; Manages study visits to ensure patient compliance with protocol activities; Disseminates research findings by drafting abstracts, presentations, and publications; Serves as liaison for scheduled Sponsor monitoring visits; Other duties as assigned

Requirements

Bachelor’s Degree required; Equivalent combination of education and experience e.g. an Associate’s degree and completion of 6 months in the Human Subject Research Coordinator Trainee program required

Nice to have

1-2 years’ experience in clinical research coordination or technology research or equivalent combination of education and experience; Knowledge of word processing and spreadsheets; Strong attention to detail and excellent interpersonal and communication skills; CITI certification