Pediatric Allergy And Immunology Human Subject Research Coordinator 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.
Job Location: 601 Elmwood Ave, Rochester, New York, United States of America, 14642 Opening:
Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40
Department: 400200 Ped Allergy/Immunology-SMDWork Shift: UR - Day (United States of America)
Range: UR URG 106 HCompensation Range: $21.78 - $30.53 The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
Responsibilities:
Coordinates the activities associated with human subject research in the department of pediatric allergy and immunology.
Essential Functions:
Coordinates and supports the administrative and logistical details required to initiate and conduct pediatric allergy and immunology human subject research, including receiving, distributing and explaining study information, such as protocol and human subject recruitment materials, to study subjects, immediate team members, and relevant others. Coordinates and supports sample kit preparation and distribution, and processing biospecimens, as part of pediatric allergy and immunology human subject research. Assists in human subject recruitment and screening activities, including reviewing study site patient databases and office records for patients that meet the protocol inclusion criteria. May participate in developing recruitment strategies for allergy patients and children/adults without allergies. May conduct telephone interviews to screen potential study candidates. Reviews medical chart history with Principal Investigator to verify atopy diagnoses. Conducts study visits to ensure research participant adherence with protocol requirements, such as taking of medications, collection of biological samples, completion of REDCap questionnaires, and/or other interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board (IRB), Sponsor, and/or any other required recipients or entities. Ensures that all data are collected and secured within approved parameters and procedures. Works with the Rochester IRB and central IRB's, when appropriate, to initiate study protocols, modify study procedures, and produce continuing review information for any assigned studies. Acts as liaison with Sponsor's Monitor to provide data clarifications, reviews study protocols, ensures thorough understanding and communication, responds to questions that arise during the study, communicates and documents adverse events as advised by the PI and ensures regulatory and other documents, such as consent forms and CRFs, are complete, accurate, and available for review. Communicates with Sponsor to clarify data queries to determine report format. Prepares for, participates in, and serves as liaison for scheduled Sponsor monitoring visits (i.e. pre-study inspection, initiation, on-going and close out visits).Keeps current with all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines and makes recommendations. Demonstrates accountability for continuous learning in accordance with Good Clinical Practice standards and guidelines. Keeps current with industry standards, best practices, and trends in therapeutic areas relevant to research studies. Makes recommendations and implements changes as appropriate. Other duties as assigned
Minimum Education & Experience:- Bachelor's degree required orAssociate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee program required
- Or equivalent combination of education and experience
- Prior experience as a phlebotomist preferred
Knowledge, Skills And Abilities:- Word processing and data analysis software preferred
- Excellent organizational skills preferred
- Experience as a phlebotomist or willing to train preferred
Licenses And Certifications:
CITI GCP and HSP preferred Dry Ice Shipping preferred The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University's Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.
