VHIR-MSCA-.003_Postdoctoral Fellowship (España)

VHIR-MSCA-.003_Postdoctoral Fellowship (España)

12 ago
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Fundacio Hospital Universitari Vall d'Hebron- Institut de recerca
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España

12 ago

Fundacio Hospital Universitari Vall d'Hebron- Institut de recerca

España

Organisation/Company Fundació Hospital Universitari Vall d'Hebron- Institut de recerca Department Research Department Research Field Biological sciences » Biology Researcher Profile Recognised Researcher (R2) Positions Postdoc Positions Application Deadline 31 Jul 2026 - 23:59 (Europe/Andorra) Country Spain Type of Contract Temporary Job Status Full-time Is the job funded through the EU Research Framework Programme? Other EU programme Is the Job related to staff position within a Research Infrastructure? No
Offer Description
Precision modelling of FHHNC using patient-derived kidney organoids for mechanistic and therapeutic discovery
VHIR is seeking an outstanding and highly motivated postdoctoral researcher to apply for a Marie Sklodowska-Curie Postdoctoral Fellowship and join the Kidney Pathophysiology Research Group.
The Marie Skłodowska-Curie Postdoctoral Fellowships (MSCA-PF) are part of the Horizon Europe programme and support postdoctoral researchers in developing an original research and innovation project through international mobility.




The programme aims to strengthen researchers’ careers through excellent science, international collaboration and interdisciplinary experience, while fostering integration in both academic and non‑academic environments. The MSCA‑PF call is highly competitive and represents an excellent opportunity to attract international talent and support researchers in consolidating their scientific careers through an ambitious mobility‑based fellowship.
The 2026 call closes on 09/09/2026 (17:00 Brussels time). For candidates applying to a European Postdoctoral Fellowship, the fellowship duration is from 12 to 24 months.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a devastating ultra‑rare renal tubulopathy caused by loss‑of‑function mutations in CLDN16 and CLDN19. The disease leads to severe magnesium and calcium wasting, nephrocalcinosis, and progressive chronic kidney disease, often culminating in renal fai

📌 VHIR-MSCA-.003_Postdoctoral Fellowship (España)
🏢 Fundacio Hospital Universitari Vall d'Hebron- Institut de recerca
📍 España

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