University of Rochester Human Subject Res Coord I in Rochester, New York
Full Time 40 hours Grade 051 Neurology - NMD M & D
8 AM-4:30 PM
Coordinates all aspects of a research study associated with human subject research. Provides assistance to the Principal Investigator and works as an integral part of the study team.
Recruits, schedules, and conducts visits for research subjects, coordinating these visits with the Principal Investigator. Resolves questions and concerns received from study subjects, triaging to the Principal Investigator as necessary.
Understands and provides training on protocols, procedures, documentation, and use of study materials to participants and team members as appropriate. Ensures compliance and follows up and communicates as needed.
May perform testing such as timed mobility tests, cognitive functions tests, etc., depending on the protocol.
Coordinates and documents dispensing and returning of study drugs/materials.
Serves as the liaison to the sponsor’s Study Monitor. Sets up and attends monitor meetings according to protocol. Prepares for and participates in scheduled Sponsor monitoring visits. Interacts with the sponsor’s team, including the Project Manager, to resolve queries from clinical research visits.
Prepares and maintains all IRB submissions. Ensures all regulatory requirements are met and documented. Updates information on Federal Clinical Trials web site.
Keeps current with study specific training, institutional certifications/policies, industry standards and best practices.
Bachelor’s degree and one year of experience in human subject research coordination; or an equivalent combination of education and experience. Knowledge of work processing and data analysis software preferred.
EOE Minorities/Females/Protected Veterans/Disabled
Job Title: Human Subject Res Coord I
Location: School of Medicine & Dentistry
Job ID: 208351
Full/Part Time: Full-Time