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Job SummaryThe Financial Compliance Data Manager II is responsible for providing assistance and support to the Claims department to collect Medicare/ Cal MediConnect (CMC), Organization Determination, Appeals & Grievances (ODAG) data from Participating Physician Group (PPG's) and Specialty Health Plans (SHP.
$102,183 - $163,492 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Case Manager Outpatient RN-CMC is responsible for the assessment, treatment planning, intervention, monitoring, evaluation and documentation on identified High Risk members. The goal of the Case Manager Outpatient CMC is to effectively manage members on an outpatient basis to assure the appropriate level-of-care is provided, to prevent in patient admission and re-admissions, and ensure that the members' medical, environmental, and psychosocial needs are met over the continuum of care.
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A minimum of five (5) plus years of experience in project management in pharmaceutical/biotechnology industry with first-hand understanding of drug development process, with prior experience in a CMC leadership role.
$160,000 - $186,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Develop CMC regulatory strategy for early-stage cell therapy products through late stage and product registration. Lead the build out CMC regulatory organization to support expanding cell therapy pipeline.
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Reviews Chemistry, Manufacturing, and Controls (CMC) information and any relevant clinical/non-clinical documentation. Demonstrated knowledge of all aspects of biotechnology and cell therapy. USC's Keck School of Medicine, Department of Medicine is seeking a dynamic individual to work on manufacturing cell and gene therapies and other biological products for internal/external users in the university's current Good Manufacturing Practices (cGMP) facility.
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Advising on CMC elements of variation / supplement packages as required. General understanding of drug development and pharmaceutical manufacturing from concept to launch including requirements for product development,manufacturing and marketing and the impact of regulatory changes on business goals/objectives.
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Eurofins BPT provides comprehensive CMC laboratory services for the world’s largest pharmaceutical and biopharmaceutical companies. The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.
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E Member of The Chartered Institute of Logistics and Transport North America (CILT); Certified Business Process Professional; Certified Management Consultant (CMC); The Institute of Asset Management (IAM.
$240,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Reconcile West business unit American Express CMC card. Maintain leases under GAAP & IFRS for RBDC in SAP ERP system. Reconcile West business unit American Express CMC card. With a culture rooted in continuous improvement, innovation, and ethical practices, we are looking for a senior accountant to help strengthen our financial operations and contribute to our growth trajectory in the accounting department.
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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
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Ability to effectively partner with Clinical, regulatory, CMC and chemistry/DMPK teams. RayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes.
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Traded biotech is seeking Sr. Associate Engineer to contribute to the Polysaccharide Downstream Pilot Plant function within the CMC team. traded biotech is seeking Sr. Associate Engineer to contribute to the Polysaccharide Downstream Pilot Plant function within the CMC team.
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Providing CMC specific scientific expertise and leadership regarding the selection, justification and qualification all vendors subsequent management of all vendor activities, from tech transfer, optimization of API, Formulations, Analytics, DP and supply chain logistics.
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With a robust set of core principles and a well-defined roadmap for sustained expansion, the company is seeking a CMC Regulatory Professional. Regulatory Specialist (CMC) Aid in executing regulatory strategies to address agency inquiries regarding CMC, dossier remediation, and product lifecycle management.
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We're looking for an individual with CAR T Cellular Therapy experience to serve as the Quality and Regulatory Affairs lead to support U.S. regulatory activities related to our cellular therapy programs, including the planning, development and execution of regulatory submissions and the overseeing of CMC Regulatory and Quality Assurance activities.
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