Post-Doctoral Fellowship in Genetic endocrinology, Establishing an epigenetic signature for Noonan syndrome (FAPESP vacancy 9917)
FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo), vacancy hosted by Faculdade de Medicina, Universidade de Sao Paulo (FMUSP/USP)
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Who can apply: No citizenship restriction is stated; the page explicitly accepts an equivalent academic CV from international applicants. Mandatory: a PhD obtained within the past 7 years (except where FAPESP rules allow) in medicine, genetics, molecular biology, biological sciences, bioinformatics or a related field; experience in… What is funded: FAPESP fellowship vacancy no. 9917: monthly fellowship of R$ 12.570,00 (the page prints “Value: R$ 12.570,00” and points to fapesp.br/valores/bolsasnopais for the current FAPESP fellowship table). The candidate applies to the host lab and the principal investigator then requests the fellowship for the selected person. Deadline: 23 October 2026.
Read the full call and apply on the official page: FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo), vacancy hosted by Faculdade de Medicina, Universidade de Sao Paulo (FMUSP/USP), official page.
Who can apply
- No citizenship restriction is stated; the page explicitly accepts an equivalent academic CV from international applicants. Mandatory: a PhD obtained within the past 7 years (except where FAPESP rules allow) in medicine, genetics, molecular biology, biological sciences, bioinformatics or a related field; experience in human genetics or rare diseases, molecular techniques, WES and variant interpretation; publications in indexed journals; scientific English; full-time work at the host institution in Sao Paulo. Apply by e-mail to [email protected] with a CV, FAPESP Curricular Summary, motivation letter (max. 2 pages), PhD proof and transcript, and two referees.
Stage dates
Deadline for submissions printed as 2026-10-23 (23/10/2026 in the Portuguese line). Apply by e-mail to the address on the page. E-mail subject: Postdoctoral Fellowship - Noonan Syndrome Epigenomics.23 October 2026
Printed start: February 2027.See the official page
Dates come from the funder's page for this round. When a round closes, the next round's dates replace these once the funder publishes them.