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The Senior Ethics & Compliance Specialist/Regulatory Support Manager is a subject matter expert on FDA regulations, the university’s policies, processes, and standards. The Senior Specialist independently oversees, advises, and manages the activities of the Regulatory Support unit and the ClinicalTrials.gov unit within OEC. The Senior Specialist is responsible for effective functional area management, long-range planning for improvement of operational efficiencies and establishing strategic directions for comprehensive regulatory consultation and clinicaltrials.gov programs.
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This is a full-time remote role and will report to the Block Regulatory Lead. They work across business groups and around the globe, spanning time zones and disciplines to develop inclusive People policies, forecast finances, give legal counsel, safeguard systems, nurture new initiatives, and more.
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Experience in advertising and promotional regulatory affairs activities through launch and commercialization are a plus. The VP, Regulatory Affairs will provide strategic regulatory expertise to support the continued development and the commercialization of acoramidis for the proposed treatment of ATTR-CM and the prevention of ATTR. This role involves collaboration with cross-functional project teams in planning and execution of development strategies while providing leadership to global regulatory submissions.
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Job DescriptionBlock is looking for an experienced Regulatory Licensing Manager with relevant international regulatory lending experience. The core mission of this role is to uphold Block's licensing and other regulatory obligations in the lending space outside of the , which are critical to our success.
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We are thrilled to be looking for a talented and skilled Cytology Applications Specialist to join our Diagnostics division, and open to candidates local or open to relocating to the Southwest region in the US. This will require you to travel up to 90% of the time.
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We are a 24-hr specialty and emergency hospital located in Berkeley, California, the heart of the San Francisco Bay Area. Our team includes two specialists in surgery, two full time and one part-time oncologist, two full time radiologists, two ophthalmologists, an exotics specialist, call-in endoscopy by a boarded internist, and an experienced and internship-trained emergency department staffed 24hrs a day.
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Our teams include Communications, Community Impact and Investment, Community Finance, CRA Strategy and Program Management, the Government and Political Affairs Group, Regulatory Relations, and Strategy and Engagement.
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Collaborate with other Exelixis stakeholders (including Clinical Development, Clinical Operations, Data Management, Medical Affairs and Regulatory Affairs) to ensure appropriate collection and handling of safety data.
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Four (4) years of full-time professional experience in editorial, newspaper, magazine, radio, television, public relations, public affairs, public information, social media, digital engagement, advertising, marketing, or similar work directly responsible for the preparation and dissemination of news and information in a variety of formats for internal and external audiences.
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This is a 100% full-time (40 hrs a week) non-exempt career position, which is paid hourly and eligible for UC Benefits. Residential and Student Service Programs (RSSP) is part of the Division of Student Affairs under the direction of the Associate Vice Chancellor/COO for Student Affairs.
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Lead and develop a team of regulatory affairs professionals in areas such as HazCom management, product stewardship, new product development support, labeling reviews, and lifecycle support activities.
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To be appointed as a Full Specialist, the candidate must have a terminal degree (or equivalent degree) in Medical Physics, Biomedical Engineering, Electrical Engineering, or a related discipline or ten or more years of relevant experience; a background in experimental NMR/MRI techniques and research studies; and be proficient in Matlab or Python.
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Partner with local market leadership and legal counsel in all matters involving legislation, planning, zoning, takings, lease contract disputes, code violations and other legal real estate and public affairs matters.
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As the Director of Regulatory Compliance (MLRO), you will be working as part of Nium’s global, dynamic Compliance team and will be reporting to the VP Compliance (US). Perform ongoing AML and OFAC risk assessments and horizon scanning for applicable regulatory requirements.
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Ambience's flagship product, Ambience AutoScribe, is a best-in-class AI medical scribe that captures the nuances of clinician-patient conversation in real-time into comprehensive medical documentation within the EMR. On average, Ambience saves 16+ hours of tedious note-taking per clinician per week.
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regulatory affairs specialist full time jobs in Oakland, CA
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