Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
. The purpose is to develop the image of the College as a community which offers a stimulating intellectual environment with a distinctive and inclusive programme of enjoyable events and to burnish its identity
-
immunofluorescence imaging. The successful candidate will support the design, optimisation, and analysis of multiplex panels to characterise the spatial distribution of immune and other cells within tumour tissues
-
a key role in supporting the delivery of the prestigious Novo Nordisk – Oxford Fellowship Programme, which funds outstanding early-career researchers in diabetes, metabolism and related fields through
-
the University of Oxford’s Department of Education, is expanding with two exciting opportunities which will help the Centre step up its programme of academic research. The Centre produces research and evidence
-
for administering the second year of the University’s Clinical Medicine programme, which is Year 5 of the standard 6-year Medicine programme and Year 3 of the 4-year Graduate-entry Medicine programme
-
We are seeking a highly motivated Postdoctoral Research Scientist to join a collaborative, translational research programme aimed at developing the first personalised mRNA vaccine
-
Astrophoria Foundation Year Programme: Classics Subject Lead The Astrophoria Foundation Year (AFY) Programme seeks to appoint a Classics Subject Lead to deliver the AFY Programme Humanities course
-
We have a new and exciting opportunity for a Postdoctoral Research Scientist to join the Pandemic Science Institute’s (PSI) growing efforts in computational vaccinology and vaccine trial design. You
-
required to research, write and distribute strategies, news releases and statements on a variety of topics, and maintain a wide range of high-level internal and external contacts. About You • Extensive
-
targets. You will join the Computational Rare Disease Genomics Team, who collectively use computational genomics to understand mechanisms underlying rare human disease to enhance diagnosis and treatment. We