University of Rochester Human Subject Research Coordinator I, CHeT - 224857 in Rochester, New York
Human Subject Research Coordinator I, CHeT
School of Medicine & Dentistry
Full Time 40 hours Grade 051 Neuro-Ctr Health & Tech/CTCC
8 AM-5 PM; OCC WKENDS
Coordinates the administrative activities associated with conducting health and technology-related 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.
Under general direction within policy guidelines and approved protocols:
Develops independent research projects utilizing technology aimed at improving health globally. Develops interactive Smart Phone applications to improve health. Coordinates the administrative activities necessary for clinical studies such as maintaining protocol and PI brochures for relevant study team members, and preparing materials for study visits, drafting and maintaining informed consent documents and the scope of work specific to projects and preparing study materials for study visits. Trains staff on details of protocol, including inclusion and exclusion criteria, informed consent procedures, and study activities.
Develops recruitment strategies and targets. Recruits and consents participants for research studies. Recruits and screens patients by reviewing study sites’ patient database and/or office records for potential study candidates that meet the proposed protocol criteria. Conducts telephone screenings of patients in order to identify potential study candidates.
Conducts remote assessments of research participants via skype and other smart phone applications. Manages study visits to ensure patient compliance with protocol activities, to document adverse events and bring to the PI’s attention and/or the IRB or sponsor as required, and to ensure that all data is collected within determined parameters.
Disseminates research findings by drafting abstracts, presentations, and publications for peer review and industry forums. Keeps current with all federal, state, sponsor and institutional policies and laws, standard operating procedures and guidelines, and makes recommendations. Demonstrates accountability for continuous learning. Keeps current with industry standards, best practices, trends in therapeutic areas relevant to research studies; makes recommendations and implements changes as appropriate.
Other duties and responsibilities as assigned.
Bachelors’ Degree and 1- 2 years’ experience in clinical research coordination or technology research; or equivalent combination of education and experience.
Knowledge of word processing and spreadsheets preferred.
Strong attention to detail and excellent interpersonal and communication skills.
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled