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Proven track record of being able to successfully interact with all levels of area, affiliate and internal authority across divisions (including Global Commercial Leaders, Forecasting, Clinical Development, HEOR, Medical Affairs and Regulatory, as well as peer equivalents in other market access teams and the market access community as a whole.
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RWE Trading Americas Inc. ("RWETA") is a dynamic energy trading company based in the heart of New York City. As a wholly owned subsidiary of RWE Supply & Trading GmbH, the globally active commercial hub of international renewable energy company RWE AG, RWETA boasts an extensive cross-commodity trading and origination mandate and access to world class energy trading infrastructure and expertise.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Provide regulatory review for reporting activities required by EU MDR (i.e. post-market surveillance, reporting, etc. With minimal oversight, the Pr. Regulatory Affairs Specialist (PRA) for the European Union Medical Device Regulation (MDR) will be responsible for supporting execution to MDR compliance plans to ensure all applicable technical files (for devices ranging from class I to class III) meet the EU MDR requirements on schedule.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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This position requires excellent interpersonal and matrix leadership skills to support effective partnerships with key internal and external stakeholders including global/regional/local HEOR leaders, Department Heads, TA Heads, CMT Leads, Development, Regulatory Affairs, and Market Access.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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RWE Analytics: Utilize advanced analytical techniques to analyze large-scale clinical data sets and derive meaningful insights that contribute to evidence generation for regulatory submissions, market access, and post-market surveillance.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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Macquarie is a global financial group providing clients with asset management, retail and business banking, wealth management, leasing and asset financing, market access, commodity trading, renewables development, specialist advisory, capital raising and principal investment.
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Responsible for developing and executing a strategic plan for the Energy Program (Hydropower, Pump Storage, and FERC Licensing) working closely with DBD. This includes coordination, developing and leading the implementation of market sector strategic plans.
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From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.
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Identify optimal reimbursement pathways for portfolio pipeline (coding/coverage/payment) Collaborate with new product development teams and clinical/regulatory colleagues to ensure health economics and market access needs are incorporated into product development plans, clinical trials and regulatory strategies Participate as contributing member on cross-functional evidence planning teams.
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Engage regularly with colleagues within Corporate Communications (Social Media & Corporate Brand Storytelling); across External Affairs (Patient Engagement & Advocacy and Government Affairs); and cross-functionally in Employee Communications, Market Access, Medical Affairs, HEOR, Legal, Regulatory and Investor Relations to understand each functions objectives and drive an aligned approach to product communications and stakeholder message harmonization.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Provide medical and scientific input to HEOR studies, RWE studies and value dossiers for market access. Provide medical and scientific input to Marketing/Market Access departments as needed.
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We’re a leader in staffing Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, HEOR, Market Access, and Sales & Marketing roles. Hematology/Oncology MSL Expansion – Top BioPharma CompanyTMAC’s direct-hire service, formerly known as TMAC Direct, is an executive search firm and Pharma’s Complete Recruiting Resource.
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Reporting directly to the head of medical affairs, the Senior Director will play a pivotal role in leading the development and execution of strategies to generate and leverage real-world evidence to support the launch, development, market access, and commercialization of Aerovate's novel cardiopulmonary therapy.
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You will: High school diploma/GED required Technical/mechanical aptitude and computer proficiency preferred Able to prioritize critical work activities and use time effectively Will Train and Certify NOTE: This position requires access to export-controlled commodities, technical data, technology, software, and services.
$18 - $25 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago
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