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): 265 Crittenden Blvd, Rochester, New York, United States of America, 14642 Opening: Worker Subtype: Regular Time Type: Part time

Scheduled Weekly Hours

20 Department: 400110 Public Health Sciences

Work Shift

UR - Day (United States of America) Range: UR URG 108 H Compensation Range: $25.14 - $35.24 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 human subject research activities for the Preventive Cardiology Research Program. Under general direction of the Principal Investigator, coordinates day-to-day study activities, supports participant recruitment and enrollment, maintains study documentation, and helps ensure compliance with federal, sponsor, and University requirements. Participates in study planning, data collection, regulatory activities, and study management while collaborating with investigators, study staff, and participants. ESSENTIAL FUNCTIONS Study Recruitment: Coordinates human subject research activities for one or more studies. Assists with participant recruitment, screening, consent, scheduling, data collection, and maintenance of study records. Participates in development of study documents, protocols, consent forms, CRFs, and study procedures. Study Coordination and Communication: Serves as the primary day-to-day contact for participants, investigators, study staff, and sponsors. Coordinates study visits, maintains communication with the PI and research team, and ensures protocol activities are completed accurately and on time. Study Management: Maintains study databases, tracking systems, documentation, and reports. Reviews study progress, monitors timelines, assists with study finances and participant payments, and supports quality assurance activities. Regulatory & Protocol Compliance: Maintains regulatory documentation and assists with IRB submissions, amendments, continuing reviews, and study closeout. Ensures adherence to protocol requirements, Good Clinical Practice (GCP), and institutional policies. Training & Operational Support: Provides protocol-specific training and guidance to research staff as appropriate. Assists with implementation of study procedures and supports consistent practices across study activities. Financial & Administrative Support: Coordinates financial tracking, budget documentation, and study-related purchasing in accordance with institutional requirements. Professional Development & Compliance: Maintains knowledge of federal, state, sponsor, and institutional regulations and completes required training. Keeps current with GCP guidance and research best practices. Other duties as assigned MINIMUM EDUCATION & EXPERIENCE Bachelor's degree and 2 years of experience in human subject research coordination required Or equivalent combination of education and experience If applicable, department specific experience required

Experience

as a Phlebotomist preferred KNOWLEDGE, SKILLS AND ABILITIES Word processing and data analysis software required LICENSES AND CERTIFICATIONS SOCRA - Certification In Clinical Research upon hire preferred Association of Clinical Research Professionals (ACRP) upon hire 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. Notice: If you are a Current Employee, please log into myURHR to search for and apply to jobs using the Jobs Hub. Your application, if submitted using this portal, cannot be moved forward. Learn. Discover. Heal. Create. Located in western New York, Rochester is our namesake and our home. One of the world’s leading research universities, Rochester has a long tradition of breaking boundaries—always pushing and questioning, learning and unlearning. We transform ideas into enterprises that create value and make the world ever better. If you’re looking for a career in higher education or health care, the University of Rochester may offer the perfect opportunity for your background and goals. At the University of Rochester, we are committed to fostering, cultivating, and preserving an inclusive and welcoming culture and are united by a strong commitment to be ever better—Meliora. It is an ideal that informs our shared mission to ensure all members of our community feel safe, respected, included, and valued.