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Responsibilities Manage all regulatory tasks and documentation for clinical trials across multiple Principal Investigators and research study teams Ensure MSK is always audit-ready by maintaining up-to-date documents, regulatory files, and ensuring protocol and policy compliance Proactively identify opportunities to contribute to the team’s success, bringing innovative ideas and solutions to the table Effectively com

Memorial Sloan Kettering Cancer Center is a cancer research and care institution whose Integrated Genomics Operation provides genomic services and expertise for research projects. The Research Assistant will operate sequencing platforms, perform library quality control and pooling, troubleshoot results, manage reagents and documentation, and collaborate with scientists and IGO teams on high-throughput workflows. Resp

Health Research, Inc. (HRI) Roswell Park Division operates the Clinical Trials Office at Roswell Park Comprehensive Cancer Center. The Regulatory Affairs Specialist ensures investigational product submissions comply with FDA regulations, advises investigators on regulatory requirements, and maintains electronic tracking of FDA submissions. Responsibilities Ensures that Roswell Park IND’s/IDE’s and other regulatory su