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Oversee our relationship with the Rare Disease Company Coalition. This role will play a key role in the evolution of our organization and lead the patient affairs strategy throughout the continuum of preclinical and clinical development to commercialization for Astria’s pipeline of programs.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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The company has a pipeline of novel and highly differentiated antibacterial and rare disease product candidates focused on patients' unmet needs with multi-drug resistant (MDR) bacterial infections.
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Our client is a biopharmaceutical company with marketed product, a robust pipeline and solid financials, focused in the Rare Disease area. Our client is a biopharmaceutical company with marketed product, a robust pipeline and solid financials, focused in the Rare Disease area.
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Demonstrated success & relationships within Endocrinology or Rare Disease. Therapy Area: Rare Disease / Endocrinology. We are now partnered with the most cutting-edge small biotech & large multi-national pharma companies focused on the future of medicine within Gene Therapy and Rare Diseases.
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Partner with commercial and medical affairs colleagues to develop global market access strategies and plans, in assigned regions, for Avidity's rare disease pipeline products through various stages of development.
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This company currently has an FDA approved product on the market with a robust pipeline in Rare Disease, Hematology and Neuroscience. Experience in Oncology/Rare Disease is preferred.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Work collaboratively with Clinical Development, Clinical Operations, Clinical Data Managers, Pharmacovigilance & Epidemiology, Regulatory, Project Management, Translational Medicine, and other staff and vendors to meet project deliverables and timelines.
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The company has a strong Rare Disease / Cardiovascular pipeline, and will be starting a Phase III as well as working on a couple of early Phase I/II studies in Q2. EDC experience - Database Builds / Study Start up / DB Locks.
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Previous FDA / Regulatory experience. I am working closely and exclusively with a specialist Biotech who will be looking to hire a Manager, Clinical Data Management soon. Experience in PII / PIII clinical trials essential.
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Prepare a business case including global revenue projections for a pre-clinical gene therapy program in a rare metabolic/liver targeted disease. One of the goals of this program is to feed a leadership pipeline of top talent for our Commercial Leadership Development Program (CLDP.
Full-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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Specialty, rare disease, and/or oncology experience strongly preferred. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people.
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Under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
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The Director of Analytics, Insights and Market Research - UShas 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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They are currently seeking a Director or Senior Director of Biostatistics (depending on experience) to be responsible for statistical activities supporting clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
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An experience in rare disease and/or with early phase development studies is a plus; Today, GENFIT has a diversified R&D pipeline covering several therapeutic areas: five programs in acute on chronic liver failure (ACLF) are in clinical stages (Phase 2) and pre-clinical stages, including hepatic encephalopathy (HE), one of the main complications of ACLF; a Phase 2 clinical program targeting cholangiocarcinoma; and a preclinical program targeting urea cycle disorders (UCD) and organic acidemias (OA.
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