UPMC Western Psychiatric Hospital is hiring a Research Coord to provide research support for studies as part of the Center for Sleep and Circadian Science, under the leadership of Dr. Jessica Levenson, Assistant Professor of Psychiatry and Pediatrics. This individual will provide key support for studies focused on the sleep and mental health of adolescents. The job purpose is to independently execute job functions to support the conduct of clinical research studies of high-risk youth and families.
The Center for Sleep and Circadian Science is committed to promoting a culture of inclusion, diversity, equity, and accountability. We believe that diverse perspectives, talents, and identities are vital to accomplishing our research mission and our mission of developing the next generation of sleep and circadian scientists. To this end, we welcome applicants with diverse backgrounds and experiences.
This position is grant funded.
Responsibilities:
Conduct day to day operations for the studies
Conduct the ethical recruitment, screening, and consenting of potential study participants
Schedule and conduct participant study visits
Track data flow for entry into project databases and analyses
Ensure accurate compensation of participants
Assist in the collection, management, processing, and analysis of data from the research assessments, interviews, and questionnaires and in the management and delivery of related equipment
Assist in reporting recruitment progress to the IRB, research teams, and National Institute of Mental Health (NIMH)
Attend and participate in all project-related meetings
Make updates to all Standard Operating Procedures for the studies
Train study staff and/or students on study procedures, database and data collection, and other study tasks as needed, and ensure IRB guidelines are followed
Support collaboration between UPMC and community recruitment sites while adhering to IRB protocol
Consult with study investigators regarding participant eligibility determinations
Communicate with community recruitment sites regarding participant eligibility and progress through the study
Maintain study files and materials to ensure compliance to regulations, including IRB and HIPAA
Support data collection and communicate any errors, deviations, or concerns with Office of Academic Computing and team members
Track adverse events and communicate with the IRB
Prepare yearly IRB renewals and any modifications that arise
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