{"schemaVersion":"jobsearcher.job.v1","id":"af9baab06a29ffee810db905","url":"https://jobsearcher.com/jobs/af9baab06a29ffee810db905","canonicalUrl":"https://jobsearcher.com/jobs/af9baab06a29ffee810db905","title":"Clinical Data Coordinator","description":"Role Overview Position: Clinical Data Coordinator\nLocation: Juno Research by JCCT, Houston, TX\nDepartment: Clinical Operations\nThe Data Coordinator supports clinical research operations by assisting Study Coordinators and the study team in executing clinical trial activities. This role ensures compliance with study protocols, Good Clinical Practice (GCP), and Standard Operating Procedures (SOPs) while maintaining confidentiality and high-quality standards.\nPosition Summary The Data Coordinator provides administrative and operational support for clinical trials, including document preparation, data entry, subject recruitment, and protocol-specific activities such as vital signs and specimen collection. The position reports to the Site Manager or Site Director and works under the direction of Clinical Research Coordinators.\nKey Responsibilities Ensure the confidentiality of clinical research volunteers and sponsors\nMaintain and advocate a high level of customer service and quality within the department\nAssist in the maintenance of Clinical Conductor\nMaintain the ERP system including preparing, filing, assisting with updates and archiving study related information\nPerform data entry and query resolution\nPrepare, handle, distribute, track and maintain clinical trial related supplies\nAssist with the pre-screening, screening, recruiting and enrollment of research subjects as authorized\nAssist with educating study volunteers on study procedures such as diary completion, electronic devices and expected outcomes in a professional and accountable manner following protocol requirements\nAssist in tracking volunteer visits in Clinical Conductor, rescheduling as needed and updating study coordinators in a timely fashion regarding missed visits or compliance issues\nPerform protocol specific activities including but not limited to medical history, vital signs, electrocardiograms and specimen collection\nRecord adverse events and concomitant medication use and follow up on open adverse events until resolution\nObtain and document study related events and data in compliance with GCP/SOPs\nCommunicate necessary volunteer information in a timely manner to study coordinator/PI on an ongoing basis\nAssure source documents/charts are prepared for future study visits\nProactively elevate issues and/or problems\nDevelop strong working relationships and maintain effective communication with study team members, investigators and practice staff\nMay collect, process and ship laboratory specimens at certain sites and or as needed\nOther duties as assigned\nEducation and Experience High school diploma or GED (required)\nBachelor’s degree (preferred)\nExperience in a clinical research setting or related environment preferred\nCertification as a Medical Assistant preferred\nAt least one year of experience in medical history, medication history, and vital signs preferred\nFamiliarity with clinical trial management systems is a plus\nSkills and Competencies Excellent communication (verbal and written) and interpersonal skills\nProficiency in Spanish and English, including the ability to speak, read, and write in both languages (preferred)\nStrong organizational and time management abilities\nDetail-oriented with high accuracy\nProficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint, SharePoint)\nKnowledge of medical terminology and clinical research concepts\nAbility to work independently and collaboratively in a team\nProblem-solving and analytical skills\nFamiliarity with electronic case report form systems (e.g., Medidata Rave, Inform, TrialKit) preferred\nAbility to manage small projects and respond to urgent needs effectively\nPhysical Requirements Ability to sit, stand, walk, reach with hands and arms, and use hands/fingers for handling or feeling\nAbility to lift and/or move up to 20 pounds\nReasonable accommodation may be provided for individuals with disabilities\nEEO Statement JCCT provides equal employment opportunities (EEO) to all employees and applicants. We value diversity at our company, and it is our policy to recruit, hire, and promote qualified individuals without regard to race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.\n\n#J-18808-Ljbffr","company":"SupportFinity","rawCompany":"supportfinity","city":"Houston","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-07-11T03:32:40.048Z","occupations":[{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"31-9092.00","title":"Medical Assistants","slug":"medical-assistants"},{"code":"15-2051.02","title":"Clinical Data Managers","slug":"clinical-data-managers"}],"industries":[{"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"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Clinical Data Coordinator","description":"Role Overview Position: Clinical Data Coordinator\nLocation: Juno Research by JCCT, Houston, TX\nDepartment: Clinical Operations\nThe Data Coordinator supports clinical research operations by assisting Study Coordinators and the study team in executing clinical trial activities. This role ensures compliance with study protocols, Good Clinical Practice (GCP), and Standard Operating Procedures (SOPs) while maintaining confidentiality and high-quality standards.\nPosition Summary The Data Coordinator provides administrative and operational support for clinical trials, including document preparation, data entry, subject recruitment, and protocol-specific activities such as vital signs and specimen collection. The position reports to the Site Manager or Site Director and works under the direction of Clinical Research Coordinators.\nKey Responsibilities Ensure the confidentiality of clinical research volunteers and sponsors\nMaintain and advocate a high level of customer service and quality within the department\nAssist in the maintenance of Clinical Conductor\nMaintain the ERP system including preparing, filing, assisting with updates and archiving study related information\nPerform data entry and query resolution\nPrepare, handle, distribute, track and maintain clinical trial related supplies\nAssist with the pre-screening, screening, recruiting and enrollment of research subjects as authorized\nAssist with educating study volunteers on study procedures such as diary completion, electronic devices and expected outcomes in a professional and accountable manner following protocol requirements\nAssist in tracking volunteer visits in Clinical Conductor, rescheduling as needed and updating study coordinators in a timely fashion regarding missed visits or compliance issues\nPerform protocol specific activities including but not limited to medical history, vital signs, electrocardiograms and specimen collection\nRecord adverse events and concomitant medication use and follow up on open adverse events until resolution\nObtain and document study related events and data in compliance with GCP/SOPs\nCommunicate necessary volunteer information in a timely manner to study coordinator/PI on an ongoing basis\nAssure source documents/charts are prepared for future study visits\nProactively elevate issues and/or problems\nDevelop strong working relationships and maintain effective communication with study team members, investigators and practice staff\nMay collect, process and ship laboratory specimens at certain sites and or as needed\nOther duties as assigned\nEducation and Experience High school diploma or GED (required)\nBachelor’s degree (preferred)\nExperience in a clinical research setting or related environment preferred\nCertification as a Medical Assistant preferred\nAt least one year of experience in medical history, medication history, and vital signs preferred\nFamiliarity with clinical trial management systems is a plus\nSkills and Competencies Excellent communication (verbal and written) and interpersonal skills\nProficiency in Spanish and English, including the ability to speak, read, and write in both languages (preferred)\nStrong organizational and time management abilities\nDetail-oriented with high accuracy\nProficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint, SharePoint)\nKnowledge of medical terminology and clinical research concepts\nAbility to work independently and collaboratively in a team\nProblem-solving and analytical skills\nFamiliarity with electronic case report form systems (e.g., Medidata Rave, Inform, TrialKit) preferred\nAbility to manage small projects and respond to urgent needs effectively\nPhysical Requirements Ability to sit, stand, walk, reach with hands and arms, and use hands/fingers for handling or feeling\nAbility to lift and/or move up to 20 pounds\nReasonable accommodation may be provided for individuals with disabilities\nEEO Statement JCCT provides equal employment opportunities (EEO) to all employees and applicants. We value diversity at our company, and it is our policy to recruit, hire, and promote qualified individuals without regard to race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.\n\n#J-18808-Ljbffr","datePosted":"2026-07-11T03:32:40.048Z","dateModified":"2026-07-11T03:32:40.048Z","hiringOrganization":{"@type":"Organization","name":"SupportFinity","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Houston","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"af9baab06a29ffee810db905"},"url":"https://jobsearcher.com/jobs/af9baab06a29ffee810db905"}}