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translation and the safety assessment of medicinal products. You will develop, integrate and share your knowledge of (primarily European) regulatory frameworks and the validation and qualification
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and the participating birth cohorts. As a postdoctoral researcher, you will: develop protocols for harmonizing cohort data and coordinate communication with cohort partners regarding data transfer
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that are researched by PhDs and Postdocs to develop HI. It is our aim to be able to use the developed metrics and methods to evaluate how well these projects provide solutions for HI as well as establish synergies
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findings at international conferences. Twenty percent of the position involves teaching responsibilities, to be agreed upon jointly with the department and the postdoc; these may include supervising BA and
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(jointly) designing and conducting studies, analysing data, preparing manuscripts, and presenting findings at international conferences. Twenty percent of the position involves teaching responsibilities
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activities will include: Building expertise: you will map out the regulatory ecosystem surrounding NAMs used for biomedical translation and the safety assessment of medicinal products. You will develop
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. We develop chemical tools to investigate these interactions to understand health and disease. The project will focus on advancing approaches in deciphering biomolecule interactions, chemical
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an essential process for life. When a cell is at a diseased state, the interaction landscape can drastically change. We develop chemical tools to investigate these interactions to understand health and
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of projects. Your qualities A PhD in quantitative mass spectrometry-based proteomics and/or structural proteomics. Experience in operating and handling a diversity of mass spectrometers independently. Strong
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Archives, whose twofold goal is to develop a theory of the queer organic intellectual while identifying the specific features of queer intellectuals’ archives. The project focuses on the place of