Puesto post-doctoral en el Instituto de Genética Humana

Hospital Universitario de Heidelberg
Hasta el 01/08/2023
2 años con posibilidad de extensión
Descripción de la oferta

We offer an exciting translational project aimed at exploring the role of random monoallelic expression in renal development and at solving the molecular cause of patients with renal hypodysplasia. For this project, we invite applications from individuals with a solid background in molecular cell biology. Prior experience with stem cells (e.g. mouse ESCs or human iPSCs), organoids, single cell RNAseq, epigenetics and kidney research is an advantage but not a prerequisite. The projects will be carried out in a stimulating work environment with scientific collaborations within the institute, across the Heidelberg life science community (e.g. EMBL, DKFZ) and worldwide.

Perfil buscado

The successful applicant will have good communication and organisational skills and a PhD in a relevant area (or be in the final stages of completion). We also invite applications from researchoriented MDs. Candidates are expected to be highly motivated and to work independently with a strong work ethic. As we are an international lab, proficiency in English language is a requirement.

Presentación de solicitudes

Applications including a cover letter, a detailed CV including a publication list and contacts of up to three referees should be sent as soon as possible to matias.simons@med.uniheidelberg.de