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The HGSC is funded from multiple National Institutes of Health sources, including the All of Us Research Program as a Genome Center, the Gregor Consortium to elucidate the genetics of rare disease funded by the National Human Genome Research Institute (NHGRI) and as a sequence technology core for the Texas Medical Center Genomic Center for Infectious Disease (GCID) established by the National Institute for Allergy and Infectious Diseases (NIAID.
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Clinical sales background with experience in rare disease, Neurology/Neuromuscular Specialist, managing large/multi-state geography, and being accountable for own business strongly preferred.
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Designs the optimal data analytics strategy for the asset taking into consideration the unique data considerations of a rare disease asset. The Director of Analytics, Insights and Market Research - US has responsibility for leading the strategy and execution of the data analytics design, acquisition/partnership, warehousing, mining and translation to commercial uptake, business reporting and insights for a pipeline asset for a rare orphan respiratory disease in the US. Additionally, this role would have oversight and management of all market research projects for the brand.
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The Company has worked on over 120 projects for Phase I-IV clinical trials across multiple therapeutic areas including cardiovascular, infectious disease, oncology and rare disease.
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The Rare Disease Account Manager will conduct business/sales with key targeted specialist healthcare providers. The Rare Disease Account Manager is responsible for developing and implementing a business/sales plan for maximizing net sales of product(s) that is aligned with the direction from commercial leadership and with all company guidelines, policies, and directives.
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We are seeking to hire a Precision Medicine Strategy Lead (PMSL) role to oversee the development and execution of biomarker strategies for Genetic Medicines involving novel therapeutic modalities across multiple disease areas including rare genetic disorders and/or neurodegenerative conditions.
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Prior experience in rare disease is required. Develop and maintain a deep understanding of Galactosemia, clinical data and commercialization strategy; and while leading by example, assure the sales force acquires and maintains deep knowledge of the disease state and clinical data.
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An early-stage growth company filled with passionate and fun teammates, dedicated to changing every life touched by rare disease. Ambit is led by a team of entrepreneurs with decades of rare and specialty disease experience and a passion to deliver data-driven innovation for our Biopharma partners.
$126,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The MSL will be responsible for key opinion leader (KOL) development in the community setting within hemolytic anemias, including, thalassemia, sickle cell disease (SCD), Pyruvate Kinase Deficiency (PK Def) and myelodysplastic syndrome (MDS) to improve patients’ lives.
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As Intercept continues to build its position as the leader in rare and serious liver disease, we are seeking a Field Reimbursement Manager (FRM). Intercept’s lead product, obeticholic acid (OCA), is a first-in-class farnesoid X receptor (FXR) agonist marketed under the brand name “Ocaliva” in the U.S., EU and Canada for the treatment of patients with primary biliary cholangitis (PBC), a rare autoimmune liver disease.
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Senior Payroll Specialist at Sumitomo Pharma in Boise, Idaho, United States Job Description Senior Payroll Specialist 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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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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Intercept is a biopharmaceutical company with a mission to build a healthier tomorrow for people living with rare and serious liver diseases. 5 years of Market Access/Sales experience; experience in Marketing, Market Access, Commercial Operations or Sales/Sales Training preferred, with a minimum of 2 years as an FRM or RAM working specifically with PBM medications.
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The CMO works closely with the Research and Development organizations driving overarching scientific leadership specifically in Hematology/Oncology, Bone Mineral, Rare Disease and Gene & Cell therapies, and in future therapeutic areas that may arise.
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Immunology, infectious disease, oncology/hematology, other specialty medicine or rare disease. immunology, infectious disease, oncology/hematology, other specialty medicine or rare disease.
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