University of Rochester Human Subject Res Coord II - 231821 in Rochester, New York
Human Subject Res Coord II Job ID 231821Location School of Medicine & Dentistry Full/Part Time Full-Time Favorite Job Regular/Temporary Regular Opening
Full Time 40 hours Grade 053 Ortho, Clinical ResearchSchedule
8 AM-4:30 PM; OCC WKNDSResponsibilities
The main duties of this individual will be to participate in protocol and consent form development, budget development, negotiation and implementation, discussions with the human subjects review board and the University's legal office, ensuring compliance with protocol procedures. They will have responsibility for overseeing administrative processes related to human subject research, maximizing efficiency in human recruitment, enrollment, and follow-up of volunteers while meeting regulatory, University and sponsor requirements for the projects. Other duties include data analysis, preparing reports on specific trials, and appropriate close out of clinical trials that are complete. May include travel to study sponsor meetings and/or travel off-site to consent and/or collect specimens/samples.
Provide professional direction for assigned projects. Organize and plan project start up, including applying for IRB, GCRC, and IBC approvals. Prepare documents for regulatory agencies including WIRB, RSRB, GCRCC, and FDA. Prepare reports including IND applications and those for FDA and IRB. Assist in design of protocols. Assist in preparation of grants for submission to government agencies.
Act as a point person for all assigned studies when Principal Investigator(s) are not available. Use clinical judgment in reviewing labs and adverse events and reporting them appropriately. Prepare serious adverse event reports.
Code data for purposes of data entry. Review and respond to data queries. Maintenance and protection of patient data.
In conjunction with Supervisor/Principle Investigator(s), prepare and maintain budgets.
Coordinate efforts of collaborating investigators. Assists Principle Investigator(s) with training to assure compliance. Represent our Center at appropriate meetings. Work with study sponsors.
Obtain informed consent, particularly as it relates to drug intervention trials. Provide detailed teaching for drug risk and potential side effects. Evaluate subject understanding of risk. Screen potential volunteers using clinical judgment in reviewing inclusion and exclusion criteria. Obtain detailed medical history. Order appropriate diagnostic tests according to protocol. Coordinate scheduling and execution of patient visits.
Perform tests according to research protocol, including phlebotomy, ECG, specimen collection, and functional measures as deemed necessary for each study protocol.
Other duties as assigned
Bachelor’s degree with major course work in an appropriate health, social or technical field required.
3 years experience in human subject research coordination required
or equivalent combination of education and experience required
Experience as Human Subject Research Coordinator I preferred
Word processing and data analysis software required
Professional Research Coordinator certification (SoCRA or ACRP) preferred
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled