Human Subject Research Coordinator Trainee

Human Subject Research Coordinator Trainee 3.9 3.9 out of 5 stars 601 Elmwood Avenue, Rochester, NY 14642 $18.65

• $26.11 an hour
• Full-time University of Rochester 1,181 reviews $18.65
• $26.11 an hour
• Full-time 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 104 H

Compensation Range:

$18.65

• $26.

11 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:

Assists with the activities associated with human subject research.

ESSENTIAL FUNCTIONS

Assists with the administrative details required to initiate and conduct human subject research, including receiving, distributing, and explaining study information, such as protocol and human subject recruitment materials, to immediate team members and relevant others. Tracks regulatory and other documents, such as consent forms and case report forms (CRFs), and ensures these are complete, accurate, and available for review. Learns and applies the details of the protocol, including inclusion and exclusion criteria, informed consent procedures, study activities, source documentation and case report form (CRFs) completion, and adverse event reporting. 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, processing biospecimens and conducting telephone interviews to screen potential study candidates. Tracks research participant adherence with protocol requirements, such as taking of medications, proper use of device 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. Tracks and documents the dispensing and returning of study materials, such as study drugs and devices. Keeps current with industry standards, best practices, and trends in therapeutic areas relevant to research studies. Other duties as assigned.

MINIMUM EDUCATION & EXPERIENCE

Associate's degree 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 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.