U

University of Rochester

Private research university in Rochester, NY

Human Subject Research Specialist 1

Full-TimePosted on 10/21/2026
$21.78 - $30.53
Mid
Bachelor's, Associate's
Rochester, NY, USA
In Person
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A bachelor's degree is required, or an associate's degree and completion of six months in the Human Subject Research Coordinator Trainee program, or an equivalent combination of education and experience.
  • Word processing and data analysis software knowledge is preferred.
  • CITI Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certification is preferred.
  • Dry ice shipping knowledge or qualification is preferred.
Responsibilities
  • Coordinate and support administrative and logistical details to initiate and conduct pediatric allergy and immunology human subject research, including receiving, distributing, and explaining study information such as protocols and recruitment materials to study subjects, immediate team members, and relevant others.
  • Coordinate and support sample kit preparation and distribution, and process biospecimens, as part of pediatric allergy and immunology human subject research.
  • Assist with human subject recruitment and screening, including reviewing study-site patient databases and office records for patients meeting protocol inclusion criteria. May help develop recruitment strategies for allergy patients and people without allergies, conduct telephone screening interviews, and review medical chart history with the Principal Investigator to verify atopy diagnoses.
  • Conduct study visits to ensure participant adherence to protocol requirements, including medication use, biological sample collection, REDCap questionnaires, and other interventions; document adverse events and report them to senior study staff, the Principal Investigator, Institutional Review Board, sponsor, and other required recipients or entities. Ensure data are collected and secured within approved parameters and procedures.
  • Work with the Rochester and central Institutional Review Boards, as appropriate, to initiate study protocols, modify procedures, and prepare continuing review information for assigned studies.
  • Liaise with the sponsor’s monitor to provide data clarifications, review study protocols, ensure thorough understanding and communication, respond to study questions, communicate and document adverse events as advised by the Principal Investigator, and ensure regulatory documents, consent forms, and case report forms are complete, accurate, and available for review. Clarify data queries with the sponsor to determine report formats, and prepare for, participate in, and serve as liaison during scheduled sponsor monitoring visits, including pre-study inspection, initiation, ongoing, and close-out visits.
  • Stay current with federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines; make recommendations; and demonstrate accountability for continuous learning in accordance with Good Clinical Practice standards and guidelines.
  • Stay current with industry standards, best practices, and trends in therapeutic areas relevant to research studies, and recommend and implement changes as appropriate.
  • Perform other duties as assigned.
Desired Qualifications
  • Prior experience as a phlebotomist is preferred.
  • Excellent organizational skills are preferred.

About the company

U

University of Rochester

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The University of Rochester is a research university with programs spanning the humanities, health care, business, education, music, engineering, and the sciences.

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