Data Manager

GENERAL PURPOSE: The position is to join a dynamic and very busy research clinic with multiple contracts with the NIH and pharmaceutical companies. Studies currently being conducted include observational studies of respiratory illnesses such as influenza and COVID19, phase 1-3 vaccine studies, studies in therapeutic agents in both adult and pediatric populations. Applicants should be able to work with research subjects under general direction and with latitude for independent judgment assume full responsibility for various clinical projects as outlined below. RESPONSIBILITIES: Data Entry: Collects, enters, and maintains study-related information in case report forms and electronic databases and reviews subject records to ensure complete and accurate data and concurrence between the data collection tools and electronic case report forms Development of Clinical Reports: Utilizes database to run reports and track subject visits.

Extracts and gathers data from human subject participants and prepares reports. Drafts adverse event logs that will be reviewed by the study coordinator prior to being sent to providers, drafts concomitant medication logs. Respond to PI and sponsor data queries. Study Preparations: Assists with the development of data collection forms, devices and other protocol-specific tools required to conduct clinical trials.

Prepares, organizes and maintains study charts (i. e. filing flowsheets and other visit documents). Assists with clinical database creation in REDCAP and other platforms and general maintenance.

Study Participant Recruitment: Assists Study Coordinator team with screening, consenting and enrolling study participants into studies of varying complexity. Conducts participant screening for clinical trials as assigned and maintains accurate screening and recruitment logs. Speak with eligible patients to assess interest and qualification for participation. Explain study and obtain informed consent and assent.

Operates computer and/or peripheral equipment; assists in preparing programs and databases related to subject recruitment. Other duties as assigned. QUALIFICATIONS: Bachelor s degree required Or equivalent combination of education and experience, e. g.

an Associate s degree and completion of 6 months in the Human Subject Research Coordinator Trainee program. Word processing and data analysis software preferred The University of Rochester is committed to fostering, cultivating, and preserving a culture of equity, diversity, and inclusion 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 status protected by law. This commitment extends to the administration of our policies, admissions, employment, access, and recruitment of candidates from underrepresented populations, veterans, and persons with disabilities consistent with these values and government contractor Affirmative Action obligations.

How To Apply All applicants must apply online. EOE Minorities/Females/Protected Veterans/Disabled Location: School of Medicine & Dentistry Full/Part Time: Full-Time Opening: Full Time 40 hours Grade 051 Medicine M&D-Infect Dis Unit Schedule: 8 AM-4:30 PM

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