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job funded through the EU Research Framework Programme? Horizon Europe - MSCA Is the Job related to staff position within a Research Infrastructure? No Offer Description The ERC-funded ALiDiM project
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motivated candidate who has a passion for in vivo Spinal Cord Injury cell/scaffold implantation treatment and neural tissue engineering research. The focus of this project is to evaluate cell transplantation
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help guide work and demonstrations in the following tasks: Firmware extraction and reverse engineering. Study, understand and analyse mobile platform applications. Design, develop and test AI-driven
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) as they move to the next phase of work involving knowledge mobilization and implementation science. Lead aspects of CHILD-BRIGHT research project(s) and program(s), where applicable. Support the
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Organization U.S. Food and Drug Administration (FDA) Reference Code FDA-CBER-2026-0041 How to Apply Connect with ORISE...on the GO! Download the new ORISE GO mobile app in the Apple App Store
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, Lung and Blood Institute (NHLBI). This exciting program is designed to support research education for cardiac, thoracic, or general surgery residents. The program will offer laboratory and clinical
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aim to address several fundamental questions in tissue and organ biology, including: How feedback between mechanics, cell fate dynamics, and geometry drives tissue patterning How 3D topological
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Instituto de Investigação e Inovação em Saúde da Universidade do Porto (i3S) | Portugal | about 2 months ago
Status Full-time Hours Per Week 35 Offer Starting Date 2 Mar 2026 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Reference Number Fellow_BI/COM_Proj2025/i3S
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MSCA Postdoctoral Fellowships @Sorbonne Université and its Alliance partners - Call for Applications
Europe Research & Innovation programme. It aims at developing the potentiel of young researchers in Europe, by funding excellent research and promoting international mobility as well as interdisciplinarity
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the genetic and developmental basis of pediatric heart disease. We analyze genetic variation in samples from patients with congenital heart defects and utilize mouse, Xenopus and cell-based models to assess