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In-depth understanding of the pharmaceutical and biotech landscape, including the regulatory environment and rare disease research, is highly desirable. Seize a fully remote experience with this dynamic full-time, exempt position requiring 40 hours per week.
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Minimum 3-5 years of experience in clinical research, with specific experience in rare disease drug development preferred. Familiarity with FDA and EMA guidance for rare disease therapies, including orphan drug designations and accelerated approval pathways.
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Specialty Pharmacies & Specialty Distributors : Understanding of the operations and role of SPs/SDs in managing the journey of patients with rare disease. Presentations : Deliver presentations on disease state, clinical, economic, access, and business topics effectively.
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Market Research: Conduct thorough market research in the rare disease therapeutic area to inform strategy development and execution. Experience in developing and launching omnichannel strategies specifically in the rare disease therapeutic area.
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ConcentricLife , part of Accenture Song, is a full-service health and wellness advertising agency spanning three distinct specialist practices that bring over 20 years of deep subject matter expertise : healthcare, rare disease, and wellness.
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The Senior Manager, HCP Marketing- Rare Disease, Friedreich Ataxia (FA) position offers an extraordinary opportunity to join a growing and evolving rare disease franchise in a therapeutic area with high unmet needs (Friedreich Ataxia.
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Our Novel Modality department covers development of treatment modalities such as siRNAs and multiclonal antibodies across multiple therapy areas within the cardiometabolic and rare disease spectrum.
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Vertex currently operates at the forefront of rare disease scientific innovation and has successfully developed and commercialized multiple breakthrough medicines for Cystic Fibrosis (CF) and Sickle Cell Disease.
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Experience with rare disease and/or pediatric trials also preferred. Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases.
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15+ years progressive Biopharmaceuticals experience, with a background in rare disease development. 15+ years progressive Biopharmaceuticals experience, with a background in rare disease development.
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Experience in rare disease strongly preferred. Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases.
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Preferred experience in specialty/rare disease. KalVista has an R&D team with an established track record in the pharmaceutical development of small molecule protease inhibitors, world-leading expertise in the role of plasma kallikrein in disease, and a management team with the capability to bring small molecules through the clinic to commercialization.
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Foster relationships with key opinion leaders in the rare disease sector. This role is pivotal in driving clinical development within the rare disease sector. In-depth knowledge of the rare disease sector.
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Background in neurological conditions and/or rare disease. Background in neurological conditions and/or rare disease. Explain and provide education related to the prescribed product, identify and recommend patient/caregiver resources that could include support groups, HUB services, specialty pharmacy, financial resources, etc.
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We are looking for experienced Business Account Executives (BAEs) with rare disease experience to promote ONPATTRO® (patisiran) in the U.S. ONPATTRO was approved in August 2018 by the FDA for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR amyloidosis) in adults.
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rare disease jobs in Cambridge, MA
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