CoMind is creating noninvasive neural technological hardware and software to augment the human brain and connect advanced artificial intelligence to the neocortex to help humans compete with the rapid advancement of AI. Backed by BACKED VC.
About the role
The Clinical Team leads the deployment of CoMind's technology into hospital environments for the first time, managing clinical sites, supporting device installations, and ensuring the smooth execution of clinical studies in partnership with clinicians.
What they're looking for
- Substantial clinical research experience, with a background in medical devices preferred
- Extensive on-site and remote monitoring experience as a sponsor-side CRA
- Strong working knowledge of GCP, ICH, FDA, and applicable global clinical research regulations
- Proven organisational and documentation skills, with the ability to manage multiple site relationships and responsibilities simultaneously
- Proficiency with EDC, eTMF, CTMS, and standard office software
More about this role
This job is based remotely in the US, and is expected to work East Coast hours. CoMind can only accept applications residing in the current states: Colorado, Florida, Missouri, Texas, Washington State, Wisconsin.
At CoMind, we are developing a non-invasive neuromonitoring technology that will result in a new era of clinical brain monitoring. In joining us, you will be helping to create cutting-edge technologies that will improve how we diagnose and treat brain disorders, ultimately improving and saving the lives of patients across the world.
The Clinical Team leads the deployment of CoMind's technology into hospital environments for the first time, managing clinical sites, supporting device installations, and ensuring the smooth execution of clinical studies in partnership with clinicians.
As Senior CRA, you will own site monitoring across CoMind's clinical programme, with responsibility spanning on-site and remote visits, in-house operations support, and study oversight. This is a hands-on role with real breadth: you will be the primary relationship owner at investigator sites while also contributing to trial management and IRB coordination internally.
Please note that this role...
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