We’re a neurotech start-up developing a breakthrough high-resolution visual prosthesis to restore useful vision for blind people. After successful animal tests, our devices are now moving toward first-in-human studies.
Role & Responsibilities
We’re looking for a motivated, science-driven, hands-on Research Associate to help run and document our clinical and preclinical studies and insure regulatory compliance. This is a great fit for someone fresh from a PhD or with a couple of years’ industry experience who wants to be involved clinical operations, GLP/ISO workflows, and how bench/animal evidence connects to human trials. ReVision being a start-up company, you should be able to work independently and be a flexible problem-solver.
Clinical
- Assist and monitor trials done by research partners
- Support data quality, keeping documentation inspection-ready
- Track safety info (AEs/SAEs) and assist with ethics/authority submissions and amendments.
Preclinical (bench & animal) – with mentoring
- Coordinate samples and paperwork for ISO 10993 biocompatibility and similar tests.
- Liaise with CROs/labs (methods, endpoints, chain-of-custody).
- Attend key procedures (implant/explant days) to observe and collect data.
- Organize raw data and help draft GLP/non-GLP study reports.
Cross-functional
- Draft and maintain study docs (protocols, monitoring plans/reports, lab manuals, SOPs) under guidance.
- Help in the setup of our QMS (ISO 13485) and learn ISO 14155, GLP/ISO 17025 basics.
- Assist with evidence packages for EU MDR and FDA pathways.
What you’ll learn here:
- Experience in how device studies are planned, monitored, and audited.
- Salary aligned with your experience and region of work
- Exciting opportunity to join a young, dynamic and hard working team, dedicated to making a real difference in the life of blind people. This is an opportunity to change the world.