At Radboudumc, you will work in a highly collaborative, interdisciplinary, and international environment. We are a leading European center for genomic medicine and rare disease research, with strong connections to clinicians, patients, and the academic + industrial analytical chemistry field. What sets us apart is our unique position at the interface of fundamental research on glycoproteomics and translational research on genetic disease applications involving clinicians and patients. This ensures that your work will have clinical relevance and impact.
You will join a group that performs (pre-)clinical research on genetic glycosylation disorders aiming to improve diagnostics, understand disease mechanisms and develop treatments. Our team consists of senior scientists, technicians, PhD students, and post-docs with multidisciplinary expertise of glycoproteomics, glycobiology, analytical chemistry, and informatics.
The position is based at Radboudumc in Nijmegen, the Netherlands. Radboudumc is internationally renowned for its research and diagnostics on a variety of genetic disorders and the impact of personalized medicine. The position is primarily housed in the department of Human Genetics with a strong collaboration with Bruker Daltonics. Our department offers an exciting working environment with enthusiastic people from many parts of the world, providing ample critical mass and a stimulating, collaborative atmosphere for high quality research.
At the department of Human Genetics, you work on the diagnosis and treatment of hereditary disorders in patients and their families. You work in the outpatient clinic or in the laboratory for diagnostic testing, where genetic, metabolic, and neurochemical analyses are performed. In addition, you contribute to research exploring the relationship between genes and disease.
As a leading, multidisciplinary department, you provide high quality genetic healthcare and contribute to scientific progress.
