University of Rochester Human Subject Res Coord I - 227970 in Rochester, New York
Human Subject Res Coord I Job ID 227970Location School of Medicine & Dentistry Full/Part Time Full-Time Favorite Job Regular/Temporary Regular Opening
Full Time 40 hours Grade 051 Psychiatry M&D ResearchResponsibilities
The Pain and Perception Lab, is conducting a search for a full time Research Coordinator. Projects will focus on understanding the neurophysiology of taste and pain perception, in healthy humans and patients with chronic pain, using behavioral testing, functional magnetic resonance imaging, and metabolic assessments.
Primary duties will include helping with IRB approvals and reviews, subject recruitment, coordination between the lab and clinical services for patients’ recruitment, testing, data management, and analysis.
25% Participant recruitment
Works with PI to develop, implement and evaluate recruitment strategies
With guidance from PI, liaises with UR clinical sites and other external sites to develop recruitment protocols
Uses independent judgment and semi-structured diagnostic interviews to identify eligible participants in clinical settings. Has ability to assess eligibility of the potential study participants via discussion with clinical providers and review of screening measures
Conducts informed consent procedures with participants and obtains written consent
25% Participant assessment and retention
Conducts assessments with study participants independently
Works with PI to establish systems for coordinating laboratory and clinical services in compliance with UR policies and procedures
Takes appropriate steps to ensure participants’ safety
Provides outreach to study participants to maximize their retention in the project
20% Data management
Works with PI to set up procedures for developing and maintaining data systems
With guidance from PI and based on study protocol, ensures the integrity and security of all study data at all times
Utilizes Python, SPSS, SYSTAT, VBA, or RealStatistics for data analyses
Assists in the development of the study database and supervises the data entry and cleaning of other study staff
Oversees direct data entry procedures via iPads or by transcribing paper data
Completes regular subject chart reviews, ensuring fidelity of documentation procedures
Develops and updates study protocols and manuals
Initiates IRB project approval process for new protocols and project amendments
Submits necessary documentation per the Data Safety and Monitoring Plan
Promotes achievement of enrollment targets via development of study specific recruitment and retention strategies
Directly trains, supervises, and mentors students or interns
10% Reporting and dissemination
Assists PI in development, writing and editing of presentations and publications of study findings
Prepares data reports to sponsoring agencies/institutions, as required.
Candidate will subscribe to the department’s goal of creating a culturally competent environment by treating research subjects and co-workers in a sensitive and caring manner. The Research Coordinator must maintain eligibility to participate in research involving human subjects by completing the Human Subjects Protection Program (HSPP) and NIH’s Good Clinical Practice training. This position also requires participation in available cultural competency training.
Minimum requirements :
Bachelor’s degree and 1 year of experience in human subject research coordination; or equivalent combination of education and experience. Knowledge of word processing and data analysis software preferred
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled