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Lead early and late-stage drug product development activities including scale-up, design of experiments (DOEs), risk assessments, and development of the integrated control strategy in partnership with other CMC functional areas, Quality, Regulatory Affairs, and Manufacturing.
$200,000 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Collaborate across Gilead Pharmaceutical Development & Manufacturing (PDM) and partner with Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Finance and Technical Development. Collaborate across Gilead Pharmaceutical Development & Manufacturing (PDM) and partner with Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Finance and Technical Development.
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Conduct government affairs work to ensure policies support equitable access to the Karius Test, including ensuring the Karius Test will be billed as Fee-For-Service in the outpatient setting (not bundled.
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Who We Are The Government Programs (GP) Team within Channel and Contract Management is responsible for managing the complexities of Government Contracting and Price Reporting to enable patient access through the federal drug programs (Medicare, Medicaid, 340B, Veterans Affairs and Department of Defense Federal Supply Schedule & TRICARE.
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Regulatory Affairs CMC – Data Administrator Contractor. Work is performed under the general supervision of more senior Regulatory Affairs CMC Systems professionals. Regulatory Affairs CMC – Data Administrator Contractor.
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Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Client therapeutic areas.
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Minimum of 7 years of experience in external affairs, advocacy, government relations, or related roles, preferably within the technology or financial services industry. Public Affairs: Represent &/or support others’ participation at events, conferences, and other forums to build relationships, foster awareness and trust in the platform and our team, and advance our programmatic and business goals.
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These programmable synthetic promoter-reporter sequences "flip on" like light switches only in dysregulated cancer cells and turn them into "factories."
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Support strategic partnerships with our cross-functional stakeholders in Medical Affairs, Global Medical Strategy and Operations, Legal, Ethics &Compliance, and R&D Quality Perform additional tasks as assigned.
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Key responsibilitiesLeads the development of the learning strategy, curriculum development, and content creation for onboarding and ongoing training of Medical Affairs scientific teams across within the virology therapeutic areas, with a focus on HIV (Treatment and Prevention) and Liver Disease (HBV, HCV, HDV, PBC.
$286,220Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Visa is a world leader in payments and technology, with over 259 billion payments transactions flowing safely between consumers, merchants, financial institutions, and government entities in more than 200 countries and territories each year.
$284,050 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Preferred Experience: 2-3 years Oncology Regulatory Affairs experience. Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial.
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This role reports to the Associate Director, Business Intelligence and will work closely with cross-functional teams, including Sales, Marketing, Market Access, Medical Affairs, Compliance, Global Technical Services (GTS), Business Planning, and GTS organizations.
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To Clinical, Manager, Monitoring, Operations, Regulatory Affairs, Project Management, Healthcare. Works cross-functionally with other Guardant Health departments (such as Bioinformatics, Clinical Operations, Regulatory Affairs, Client Services, etc.
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Worldwide, the Volkswagen Group has a long tradition of dramatic innovations.
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affairs job Title: sr Company: Csl Behring in San Mateo, CA
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