{"schemaVersion":"jobsearcher.job.v1","id":"ee426510f7fa74ee9daf9ac6","url":"https://jobsearcher.com/jobs/ee426510f7fa74ee9daf9ac6","canonicalUrl":"https://jobsearcher.com/jobs/ee426510f7fa74ee9daf9ac6","title":"Remote Clinical Project Manager","description":"This job is based remotely in the US, but you should be based in an Eastern or Central Time zone.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 RoleThe 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 Clinical Project Manager, you will own the planning, execution, and oversight of assigned clinical studies, working cross-functionally with clinical operations, regulatory, data science, and investigator sites to ensure studies are delivered on time, within budget, and in full compliance with applicable regulations.Please note that this role will require approximately 20% travel, depending on study needs.Responsibilities:Develop and maintain clinical project plans, timelines, and budgets; lead site feasibility assessments, selection, and CTA negotiations for assigned studiesPrepare and review key study documents including protocols, ICFs, CRFs, and study manuals in accordance with ISO 14155, FDA/ICH guidelines, and CoMind SOPsOversee site initiation, monitoring, and close-out visits, ensuring protocol adherence and data quality; track enrollment and KPIs and proactively mitigate risks to study timelinesReview monitoring reports and drive timely resolution of site issues, deviations, and CAPA activitiesManage clinical data activities including CRF completion, query resolution, and data cleaning in collaboration with data managementEnsure study conduct compliance with 21 CFR Parts 812, 50/56, ISO 14155, and GCP; support internal and external audits and FDA inspections as requiredAuthor and review clinical study reports, periodic safety reports, and clinical evaluation reports; provide regular study status updates to senior management and cross-functional stakeholdersAI 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:3-6 years of clinical research experience, with at least 2 years in medical device clinical trialsDemonstrated knowledge of FDA regulations (21 CFR 812), ISO 14155, and GCP guidelinesHands-on experience managing clinical sites and/or CRO relationshipsProficiency with EDC, eTMF, CTMS, and standard office softwareStrong communication, organisational, and documentation skills with the ability to manage multiple studies simultaneouslyNice to have:Familiarity with neurology, neurocritical care, TBI, or ICU-based clinical settingsExperience authoring or contributing to clinical study reports or clinical evaluation reportsBenefits: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","company":"Comind","rawCompany":"comind","isRemote":true,"isActive":false,"createdAt":"2026-06-13T17:54:54.204Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"15-1299.09","title":"Information Technology Project Managers","slug":"information-technology-project-managers"}],"industries":[{"code":"621112","title":"Offices of Physicians, Mental Health Specialists","slug":"offices-of-physicians-mental-health-specialists"},{"code":"621498","title":"All Other Outpatient Care Centers","slug":"all-other-outpatient-care-centers"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Remote Clinical Project Manager","description":"This job is based remotely in the US, but you should be based in an Eastern or Central Time zone.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 RoleThe 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 Clinical Project Manager, you will own the planning, execution, and oversight of assigned clinical studies, working cross-functionally with clinical operations, regulatory, data science, and investigator sites to ensure studies are delivered on time, within budget, and in full compliance with applicable regulations.Please note that this role will require approximately 20% travel, depending on study needs.Responsibilities:Develop and maintain clinical project plans, timelines, and budgets; lead site feasibility assessments, selection, and CTA negotiations for assigned studiesPrepare and review key study documents including protocols, ICFs, CRFs, and study manuals in accordance with ISO 14155, FDA/ICH guidelines, and CoMind SOPsOversee site initiation, monitoring, and close-out visits, ensuring protocol adherence and data quality; track enrollment and KPIs and proactively mitigate risks to study timelinesReview monitoring reports and drive timely resolution of site issues, deviations, and CAPA activitiesManage clinical data activities including CRF completion, query resolution, and data cleaning in collaboration with data managementEnsure study conduct compliance with 21 CFR Parts 812, 50/56, ISO 14155, and GCP; support internal and external audits and FDA inspections as requiredAuthor and review clinical study reports, periodic safety reports, and clinical evaluation reports; provide regular study status updates to senior management and cross-functional stakeholdersAI 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:3-6 years of clinical research experience, with at least 2 years in medical device clinical trialsDemonstrated knowledge of FDA regulations (21 CFR 812), ISO 14155, and GCP guidelinesHands-on experience managing clinical sites and/or CRO relationshipsProficiency with EDC, eTMF, CTMS, and standard office softwareStrong communication, organisational, and documentation skills with the ability to manage multiple studies simultaneouslyNice to have:Familiarity with neurology, neurocritical care, TBI, or ICU-based clinical settingsExperience authoring or contributing to clinical study reports or clinical evaluation reportsBenefits: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","datePosted":"2026-06-13T17:54:54.204Z","dateModified":"2026-06-13T17:54:54.204Z","hiringOrganization":{"@type":"Organization","name":"Comind","sameAs":"https://jobsearcher.com"},"jobLocationType":"TELECOMMUTE","applicantLocationRequirements":{"@type":"Country","name":"US"},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"ee426510f7fa74ee9daf9ac6"},"url":"https://jobsearcher.com/jobs/ee426510f7fa74ee9daf9ac6"}}