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Performs and documents periodic radiation safety and calibration surveys of all CT, Mammography, Radiography and Fluoroscopy equipment, in compliance with radiation safety and regulatory agency requirements.
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Tasks may include providing support to technical staff and project managers on permitting, site and impact assessment, restoration, land use management plans, public involvement, and environmental regulatory compliance assignments.
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Claims Examiner I is responsible for reviewing and processing medical, dental, vision and electronic claims in accordance with state, federal and health plan regulatory requirements, department guidelines, as well as meet established quality and production performance benchmarks to include research and review of applicable documentation.
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The potential for international trade of hydrogen, with shipping in various forms, including liquefied gas, or ammonia as a hydrogen carrier, and a rapidly changing landscape with technology, policy and regulatory innovation.
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Preferred: Possession of current school security officer training certificate pursuant to California Education Code Section 72330.5 and Business and Profession Code Section 7583.45, as provided by the Bureau of Security and Investigative Services of the California Department of Consumer Affairs, or ability to successfully complete said training within one year after hire.
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As a Senior FP&A Analyst, you will play a pivotal role in their Finance team, acting as a strategic business partner to the Chief Product Officer (CPO), Chief Information Officer (CIO), and Chief Information Security Officer (CISO).
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Knowledge of and experience in selling biometrics, regulatory submissions, and regulatory operations will be a distinct advantage. MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Aseptic practices and clean room operations: Advanced knowledge of GMP, FDA and EMA regulatory requirements applicable to Biologics including Gene/Viral therapy products focusing on Downstream Operations.
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Desired: 1) Human subjects research experience including knowledge of IRB, NIH, HIPAA and other regulatory rules and requirements, 2) Experience collecting Magnetic Resonance Imaging (MRI) data from human subjects, 3) Proficiency with Microsoft Office programs.
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Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
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The Sr. Accounting Manager is responsible for all areas relating to financial reporting. This position reports to the Sr. Director of Corporate Finance or another management personnel that the President of the Company may designate.
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The role of this team is to convey the status of the Call Center (Tier 1), National Consumer Affairs (NCA, Tier 2 and 3), and Buyback (collectively known as “Customer Connect”) operations and customer satisfaction in an accurate and efficient manner.
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Strong business acumen and experience working with various internal business partners (especially Sales, Marketing, Medical Affairs, Clinical, Regulatory, Legal, and Government Affairs staff) to provide insight into key market access issues.
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Solid knowledge of regulatory requirements governing medical record processing, charge capture, and release of information. Document Imaging/Clinical Records Management/Data Integrity:Performs all scanning, indexing and review of documents, adhering to policy, standard operating procedures and service level agreements with clinical departments.
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Collaborate and coordinate across multiple functions, including product management, convention management, clinical affairs, legal and regulatory affairs, to ensure timely and accurate completion of projects.
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regulatory affairs jobs Title: sr regulatory associate in Irvine, CA
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