# MVA Society jobs and careers

> 0 open roles at MVA Society as of October 23, 2026. Source: https://www.thejobsmap.com/company/mva-society

The MVA Society has been set up as a patient advocacy site to establish a focal point for the ultra-rare genetic condition Mosaic Variegated Aneuploidy syndrome. We believe this is the first (and only!) dedicated organisation and site for MVA. The aims of the MVA Society are 3 fold: 1. Act as a patient advocacy support and information resource 2. Build a community of practise and patient cohort 3. Investigate research into screening, surveillance and treatment of MVA We would love to hear from you – please feel free to contact us on info@mvasociety.org George's Story The Founder, Jonathan Bracey (JB) set up this charity after his son, George, was diagnosed with this condition in August 2023. George was 2 years old at the time. He was diagnosed under the R14 genome sequencing testing carried out under the NHS in London. However, the information and dedicated support for MVA was extremely limited, so he decided to set up The MVA Society to redress that balance.

## Key facts

| | |
|---|---|
| Open roles | 0 |
| Headquarters | United Kingdom |
| Employees | 1 to 10 |
| Website | https://mvasociety.org |

## Common questions

### Is MVA Society hiring right now?

MVA Society has no open roles listed as of October 23, 2026. Roles appear here as soon as they are posted on MVA Society's careers site.

### Where is MVA Society headquartered?

MVA Society is headquartered in United Kingdom.

### How do I apply for a job at MVA Society?

Pick a role on MVA Society's TheJobsMap page and select Apply. Every listing links to the original posting on MVA Society's own careers site, so you apply directly with the employer.
