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The company has a pipeline of novel and highly differentiated antibacterial and rare disease product candidates focused on patients with unmet need associated with multi-drug resistant (MDR) bacterial infections.
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Some of our programs are wholly owned, and some are advancing with partners including Alexion, AstraZeneca Rare Disease; Novartis Pharma AG; Neurocrine Biosciences, Inc.; and Sangamo Therapeutics, Inc. For more information, visit www.
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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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Dr. Amy Dickey is seeking to hire a clinical research coordinator for diverse and innovative projects related to the study of porphyria, a family of rare genetic diseases affecting the production of heme.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Lead due diligence and scientific assessment for rare disease therapeutic areas. Business Development Director | Head of Business Development | Licensing Director | Pharmaceutical | Biotechnology.
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Would you like to be part of a dynamic and exciting Technology Operations Team delivering a high level of service that has a direct impact on the lives of cancer and rare disease patients worldwide.
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Alexion, AstraZeneca Rare Disease is seeking a highly motivated co-op with educational experience in Regulatory Affairs. Alexion, AstraZeneca Rare Disease is seeking a highly motivated co-op with educational experience in Regulatory Affairs.
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Experience with rare disease development or related science focus is required. Thorough understanding of rare muscle diseases, with experience integrating novel endpoints and biomarkers into clinical trials.
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Relevant experience in the Gastrointestinal therapeutic and/or rare disease area a plus. Ironwood is also advancing apraglutide, a next-generation, long-acting synthetic GLP-2 analog being developed for rare gastrointestinal diseases, including short bowel syndrome with intestinal failure, as well as several earlier stage assets.
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Experience in launching in rare disease (i.e. neurology and/or immunology) is required. Scientific communication and education strategy e.g. publications strategy, congress strategy, HCP interaction strategy, and the scientific communication platform for the disease area / brand(s.
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Manage the system integration of existing Salesforce modules (Salesforce CPQ) and complementary tools and add-ons (Groove, Showpad, Xactly) and pro-actively suggest and implement new solutions to best fit the growing needs of the Company.
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And has already enabled us to provide genetic diagnoses to more than 2,000 rare disease families. Rare Genomes Project. Genomics and DNA sequencing data analysis. Docker, Kubernetes, a major cloud provider (AWS, GCP, Azure.
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At Alexion, AstraZeneca Rare Disease, we are innovators, leaders, and collaborators. Fluency in English and ideally additional European LanguagesRecent track record of successfully overseeing product launches in local market, ideally for rare or orphan disease(s); has successfully worked in a competitive environment.
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The company's areas of focus are rare genetic diseases, multiple sclerosis, cardiovascular disease, and endocrinology. Our parent company has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, rare diseases, consumer healthcare, emerging markets and animal health.
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Inozyme Pharma, Inc. (Nasdaq: INZY) is a clinical-stage rare disease biopharmaceutical company developing novel therapeutics for the treatment of diseases of abnormal mineralization impacting the vasculature, soft tissue, and skeleton.
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rare disease jobs in Waltham, MA
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