Sr Human Subject Research Spec - Ped Allergy

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 (Full Address):

601 Elmwood Ave, Room 48104, 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-SMD

Work Shift:

UR - Day (United States of America)

Range:

UR URG 110

Compensation Range:

$61,000.00 - $85,400.00

_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:

The Senior Human Subject Research Specialist will work with minimal direction of the Principal Investigator and provide study coordination services for complex sponsor and government funded research involving newborns, infants, children and their families. With broad latitude for autonomy and independent judgment, the Senior Specialist is responsible for implementation of study protocols, identifying and consenting research subjects, acting as resource for research subjects and their families, supervising study visits at the Clinical Research Center (CRC), clinical areas, and home-visits, collecting data at study visits, and maintaining study database. The position will be expected to organize multiple projects, allocate resources, monitor progress, and meet multiple deadlines. Coordinates, monitors, and oversees all phases of complex grants (NIH and other agencies). There is potential for travel to investigator meetings and conferences. Responsibilities will include but not limited to training and managing study staff, regulatory and fiduciary oversight, and representing the Principal Investigators in their absence.

Work on an independent level, making primary decisions related to research specific implementation. Work collaboratively in the development of research protocols and consents. Maintain appropriate IRB (RSRB or WIRB) approval and documentation. Provide knowledge and skills to successfully maintain proper study activities. Maintain continuous relations with study team and principal investigator. Demonstrate ability to develop and maintain good clinical practice, division goals and objectives and utilize expert skill and knowledge to deliver safe and thorough research subject care. Demonstrates IICARE values in each of the major responsibilities.

**ESSENTIAL FUNCTIONS

Human Subject Recruitment & Management**

• Direct the comprehensive process of subject recruitment, screening, enrollment, and follow-up for complex clinical studie...

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis.