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Rare disease and / or complex therapy administration experience. The Associate Patient Support Training Director is responsible for leading the development and delivery of the training curriculum to support the patient support team, new hire training, onboarding, and role specific supplemental development training.
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Experience in the rare disease field or/and pediatric endocrinology is a plus. Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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That’s how we tackle rare disease. Every day at BioLife, we feel good knowing that what we do helps improve the lives of patients with rare diseases. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd.
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Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets. To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group research, develops and markets innovative drugs in its three therapeutic areas: AIR (products and services that promote respiration, from new-born to adult populations), RARE (treatment for patients with rare and ultra-rare diseases) and CAR E (products and services that support special care and consumer-facing self-care.
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We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification , a recognition of high social and environmental standards. We are a B Corp and Benefit company awarded Top Employer status for six consecutive years and certified as a Great Place to Work.
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5+ years of specialty/rare disease/biologics sales experience, neurology strongly preferred. As part of that team, the Territory Business Manager (TBM) for the Neurology Franchise will drive demand generation through a focused approach on healthcare professionals, academic institutions, and specialty pharmacy/infusion providers.
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2+ years recent Specialty and/or Rare Disease experience required. Demonstrate deep marketplace, therapeutic, product and disease expertise based on thorough understanding of rigorous scientific principles and data, including mechanism of action, indications, efficacy, safety, etc.
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Treatment for patients with rare and ultra-rare diseases) and. Prior experience working on a launch product in a respiratory disease is preferred. In-depth knowledge of respiratory diseases with expert insight to drive the disease vision through rigorous scientific debates with medical thought leaders.
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Each year 25,000 babies with rare disease get lifesaving treatments as a direct result of our newborn screening capabilities. Each year 25,000 babies with rare disease get lifesaving treatments as a direct result of our newborn screening capabilities.
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B Corp Certification , a recognition of. Oversee chargeback operations and communication with wholesalers. Mktg, Market Access, Bus. Excellence & Med. Affair. Experience with pharmaceutical industry contract management and rebates applications (i.e., iContracts, Model N.
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Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical patient need spanning psychiatry & neurology, oncology, urology, women’s health, rare disease, and cell & gene therapies.
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We are working on a Vice President, Global Regulatory Affairs opportunity with a growing pharmaceutical company that is in the areas of rare-disease/biologics/immunology/nephrology. We are working on a Vice President, Global Regulatory Affairs opportunity with a growing pharmaceutical company that is in the areas of rare-disease/biologics/immunology/nephrology.
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As a Clinical Scientist/Associate Medical Director, Clinical Development, this candidate will work cross-functionally to develop strong relationships with key stakeholders within Clinical Development, Clinical Operations, Regulatory Affairs, and Pharmacovigilance to support ongoing clinical trials and the lifecycle of the drug candidate.
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Represent the medical team in clinical study team meetings, contributing medical/scientific knowledge to cross‐functional teams; liaise with other departments for data review in clinical and safety databases.
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Chiesi USAChiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets. Direct experience with rare disease drug development a plus.
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rare disease jobs in Raleigh, NC
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