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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.
The University 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. 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.
This position serves as a vital link within the Neurology Department, specifically supporting the NMD M & D team. The role focuses on coordinating activities associated with human subject research, with a specialized emphasis on clinical projects involving patients with muscular dystrophy, specifically myotonic dystrophy.
You will be an integral part of a research team dedicated to advancing medical science. Your work will support clinical trials evaluating genetic therapies targeting the root cause of the disease, as well as observational studies leveraging a remote research platform developed by the Myotonic Dystrophy research team. A key aspect of the role involves assisting in the enhancement and expansion of this remote research platform, ensuring seamless operations between the research team, the Principal Investigator, and study participants.
This full-time position is based at the University of Rochester, located at 601 Elmwood Ave, Rochester, New York, 14642.
Work model: On-site
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Experience with word processing and data analysis software. Prior experience as a Phlebotomist. REDCAP experience. CLASP, SOCRA, or ACRP certification.
Skills: Word Processing, Data Analysis, Phlebotomist, Redcap, Clasp, Socra, Acrp.
Education: Bachelor's degree required, or Associate's degree with 6 months trainee program, or equivalent experience; Associate's degree required with completion of 6 months in Human Subject Research Coordinator Trainee program.