Human Subject Research Spec I- TAR

University of Rochester • Rochester, NY

2d • Onsite

About The Position

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.

This position coordinates the activities associated with human subject research. Essential functions include coordinating administrative details, conducting study visits (including obtaining informed consent and accompanying participants for behavioral and MRI imaging visits), administering child and parent questionnaires, assisting with neurocognitive testing, assisting in human subject recruitment and screening activities, reviewing patient databases and office records, conducting telephone interviews, reviewing medical chart history, documenting and reporting adverse events, and ensuring data collection and documentation compliance. Other projects and job duties as assigned.

Requirements

• Bachelor's degree required or Associate’s degree and completion of 6 months in the Human Subject Research Coordinator Trainee program or equivalent combination of education and experience required

Nice To Haves

• Word processing and data analysis software preferred

Responsibilities

• Coordinates the administrative details required to conduct human subject research, including receiving, distributing, and explaining study information, scheduling and logistics for researchers and study participants
• Conducts study visits, including obtaining informed consent, and accompanying participants for behavioral and MRI imaging visits
• Administers child and parent questionnaires, assists with neurocognitive testing
• Assists in human subject recruitment and screening activities, including reviewing patient databases and office records for patients that meet the protocol inclusion criteria
• Will conduct telephone interviews to screen potential study candidates
• Reviews medical chart history with Principal Investigator to verify inclusion criteria are met before enrollment
• Document adverse events and report to senior study staff, PI, Institutional Review Board (IRB), Sponsor, and/or any other required recipients or entities
• Ensures all data are collected and secured within approved parameters and procedures and all documents are in compliance annually
• Other projects and job duties as assigned

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level