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Remote Clinical Research Coordinator (PST/EST/CST Timezone) at Indeed. . Location: Mexico City. Mexico. Remote Clinical Research Coordinator (Remote – . PST/CST/EST Hours). . LOCATION: Mexico. . Job Description:. . . . . . Remote Clinical Research Coordinator. . Location:. . Remote – U.S. Time Zones Preferred. . Client:. . This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing.. . About the Role:. . UniTriTeam is seeking a Remote Clinical Research Coordinator (CRC) to support one of our clinical research site clients. This position is fully remote and does not involve in-person patient interaction, but will require coordination and facilitation of remote patient visits, as well as all behind-the-scenes clinical trial support. The ideal candidate has strong communication skills, is detail-oriented, and has experience using CTMS platforms such as CRIO or Clinical Conductor.. . Key Responsibilities:. . . Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines.. . Support and facilitate remote patient visits, including scheduling, documentation, and follow-up.. . Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone.. . Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution.. . Assist with regulatory document management and remote IRB submissions and updates.. . Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections.. . Serve as a virtual liaison with sponsors, CROs, and internal site teams.. . Support study startup and closeout tasks, including remote collection and verification of essential documents.. . Monitor visit schedules and ensure all subject documentation is complete and up to date.. . . Required Qualifications:. . . 2+ years of experience in clinical research coordination or clinical operations.. . Strong understanding of GCP, ICH, and FDA regulatory requirements.. . Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred.. . Fluent in English – both verbal and written communication required.. . Comfortable working independently in a fully remote setting across multiple time zones.. . Highly organized with strong attention to detail and documentation accuracy.. . Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.).. . . Preferred Qualifications:. . . Associate or Bachelor’s degree in health sciences or related field.. . Clinical research certification (e.g., ACRP, SoCRA).. . Prior experience supporting multi-site trials remotely.. . Bilingual proficiency is a plus.. . . Work Schedule:. . Full-time (Remote), U.S. time zones (EST to PST). . Perks of Working with UniTriTeam:. . . Work with a mission-driven organization transforming the clinical research industry.. . Fully remote work environment with global team collaboration.. . Exposure to innovative research sites and a wide variety of protocols.. . Professional development and growth opportunities.. . Supportive and inclusive team culture.. . . . . . . Why Join Us?. UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from:. . . A collaborative and supportive work environment. . Opportunities for professional growth and advancement. . A chance to be part of meaningful research initiatives that change lives.