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10+ years of relevant experience in a Trading Prop Shop, Market-maker, Asset Manager, Hedge Fund, or Brokerage Environment. We are looking for a Head of Market Making who will drive growth of FalconX's Market Making and Liquidity Services business, including the development and nurturing of external crypto projects and partners, as well as internal/external operations (P&L, hiring, etc.
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Prior experience in partnering with market-leading COTS products used by financial institutions - Moody's Risk Advisor, SAS, Actimize, Mantas, Axiom SL. Strong understanding of Regulatory Compliance in the areas of Investment Banking, Asset Management, Wealth Management, Market Infrastructures, P&C insurance, and L&A.
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Demonstrated experience working with routinely collected data (claim databases, electronic medical (health) records, registries), and various structured and possibly unstructured data sources in the healthcare sector within pharmaceutical companies’ settings in commercial market access, medical affairs, scientific affairs and/or R&D environment.
$271,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our client, a major bank in Iselin, NJ is looking for Sr Application Support Engineer for Market Operations Support group. Supporting applications under Market Operations Support group.
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Make an hourly wage of up to $55 as a Licensed Practical Nurse (LPN) throughout Somerset County, New Jersey, with the peace of mind that flexible schedules and W2 employment enable. Need a day off to help chaperone your child's class field trip to the Princeton University Art Museum.
$55 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Ensure a close working relationship with all US cross-functional Rare Disease team members, including field-based counterparts and home office-based team members, legal, regulatory, market access individuals, medical/clinical operations.
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5-7 years of pharmaceutical and or life sciences marketing experience; additional pharmaceutical experience in sales, medical affairs, and market access a plusExperience with marketing and/or selling biologics within at least two of the following disease areas is REQUIRED: dermatology, immunology, rheumatology.
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This role will be responsible for leading projects from definition through launch phase, gathering customer feedback and market intelligence, and managing product lifecycle and pricing. Demonstrated ability to conduct market research and develop business cases.
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This position is responsible for independently providing innovative and strategic legal support and solutions as a market access attorney and the primary legal advisor for market access and contract and pricing departments supporting U.S. approved (or to be approved) products including, but not limited to, areas of GPO/PBM and trade/distribution agreements, Medicare, Medicaid, product pricing, and government price reporting.
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Wakefern Food Corp. is the largest retailer-owned cooperative in the United States and supports its co-operative members' retail operations, trading under the ShopRite®, Price Rite®, The Fresh Grocer®, Dearborn Markets®, Fairway Market®, and Gourmet Garage® banners.
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We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. The Director, Human Resources will partner with the Executive Director and COO of Bausch Health and serve as the HR Business Partner for the Global Manufacturing, Facilities, HSE, Quality, IT and Business Development organizations.
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The Senior Director, Strategy and Operations is responsible for managing all aspects of market access operations, including 3PL processes, analytics, contracting and government pricing. Lead the market access strategy and operations function.
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Are you pursuing an MBA, MA, MS, MPH, PharmD, PhD in Economics, Epidemiology, Psychology, Public Health, Pharmacy, Health Outcomes Research, Health Services Research, or other market access related program.
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Our clients are enterprises as diverse as sophisticated financial institutions and start-ups, global public firms, and middle-market companies, as well as high net worth individuals, family offices, not-for-profit organizations, and entrepreneurial ventures across a variety of industries.
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Responsible to work on Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post-market clinical follow-up (PMCF), Summary of Safety and Clinical Performance (SSCPs), state of the art (SOTA) on medical devices, post market surveillance reports, Periodic safety update reports, Literature reviews, Protocol development, Clinical study reports, and Investigator’s brochure, Clinical Evidence Summaries, Risk-benefit analysis reports for medical devices as per MDD and MDR requirements.
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