Senior CRA

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 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. 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 will require approximately 50% travel, depending on study needs. Responsibilities: Conduct qualification, initiation, interim, and close-out monitoring visits (on-site and remote) in accordance with GCP, ICH, the study protocol, and CoMind SOPsPerform source data review and verification, manage data query resolution, and evaluate site performance, protocol adherence, and enrollment progressIdentify and escalate site issues, deviations, and risks; support CAPA development and inspection and audit readiness activitiesBuild and maintain strong relationships with investigator sites, providing training, guidance, and support to ensure study quality and continuityPrepare, submit, and track IRB maintenance submissions including continuing reviews, amendments, and safety updates, coordinating directly with central IRBs to ensure timely approvalsMaintain Trial Master File quality, support regulatory submissions and site activation activities, and manage IP logistics and accountability documentationAI is fundamental to our culture -- it's not just a tool, but a core part of how we work, collaborate, and innovate. We expect all team members to embrace AI in their daily work and continuously find new ways to use it effectively. Skills & Experience: Substantial clinical research experience, with a background in medical devices preferredExtensive on-site and remote monitoring experience as a sponsor-side CRAStrong working knowledge of GCP, ICH, FDA, and applicable global clinical research regulationsProven organisational and documentation skills, with the ability to manage multiple site relationships and responsibilities simultaneouslyProficiency with EDC, eTMF, CTMS, and standard office software Nice to have: Experience with early feasibility studies, NSR studies, or IDE-regulated frameworksFamiliarity with neurology, neurocritical care, TBI, or ICU-based clinical settingsExperience coordinating IRB submissions and managing regulatory documentation at a sponsor level. Benefits: Company equity planAnnual Unlimited PTOHealth insurance plan - CoMind contributes 50% to the monthly premium (with the Blue Cross Network)Dental insurance (50% Employer Contributions to individual policy)Vision insurance (50% Employer Contributions to individual policy)401k plan with an employer match up to 3%Mental health resources Compensation Range: $130K - $145K