- Cardinal Health (Albany, NY)
- **_What Regulatory Submissions Operations contributes to Cardinal Health_** Regulatory Submissions Operations uses specialized technology and knowledge ... and compile paper and electronic documents related to the pharmaceutical industry regulatory submissions throughout each phase of drug development and though… more
- University of Rochester (Rochester, NY)
- …the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE: The Sr . Clinical Trials Project Mgr. role supports the URCC NCORP ... culture. + Monitor compliance with program guidelines, deadlines, and regulatory requirements, ensuring accountability across the Research Base. + Work… more
- Mount Sinai Health System (New York, NY)
- …and regulatory staff in the preparation of new protocol submissions , protocol amendments, and renewals of ongoing clinical trials. 6. Obtains informed ... under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects,… more
- Echelon Supply & Service (Liverpool, NY)
- …Overview: We are seeking a proactive and detail-oriented Quality / ISO Coordinator to lead quality assurance initiatives and manage our Quality Management System ... skills, a collaborative mindset, and experience interfacing with customers and regulatory bodies. US Citizenship is required. Key Responsibilities: Quality Assurance… more
- City of New York (New York, NY)
- …history. This investment, coupled with a commitment to reduce administrative and regulatory barriers, is a multi-pronged strategy to tackle New York City's complex ... general contractors, and other government agencies; - Reviewing and coordinating submissions of required CEQR, NEPA and other environmental review reports; -… more