Remote Clinical Research Coordinator (PST/EST/CST Timezone)

<p><strong>Remote Clinical Research Coordinator (Remote – </strong><strong>PST/CST/EST Hours)</strong></p> <p><strong>LOCATION: Mexico</strong></p> <p class="css-1655dm5 e1wnkr790">Job Description:</p> <div class="css-1dhd1xm eu4oa1w0"> <div class="jd-appended-job-description"> <div class="jd-section-employer"> <div class="jd-description-text"> <p>Remote Clinical Research Coordinator</p> <p>Location:</p> <p>Remote – U.S. Time Zones Preferred</p> <p>Client:</p> <p>This position is in partnership with a client of UniTriTeam, a leader in clinical research support and global staffing.</p> <p>About the Role:</p> <p>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.</p> <p>Key Responsibilities:</p> <ul> <li>Coordinate day-to-day clinical trial operations in a remote capacity, ensuring compliance with study protocols and regulatory guidelines.</li> <li>Support and facilitate remote patient visits, including scheduling, documentation, and follow-up.</li> <li>Patient Recruitment support to include inclusion/exclusion understanding and qualifying patients for studies via phone.</li> <li>Maintain accurate and timely data entry in EDC and CTMS systems; manage query resolution.</li> <li>Assist with regulatory document management and remote IRB submissions and updates.</li> <li>Prepare for and participate in remote sponsor/CRO monitoring visits, audits, and inspections.</li> <li>Serve as a virtual liaison with sponsors, CROs, and internal site teams.</li> <li>Support study startup and closeout tasks, including remote collection and verification of essential documents.</li> <li>Monitor visit schedules and ensure all subject documentation is complete and up to date.</li> </ul> <p>Required Qualifications:</p> <ul> <li>2+ years of experience in clinical research coordination or clinical operations.</li> <li>Strong understanding of GCP, ICH, and FDA regulatory requirements.</li> <li>Proficiency with CTMS platforms – CRIO or Clinical Conductor strongly preferred.</li> <li>Fluent in English – both verbal and written communication required.</li> <li>Comfortable working independently in a fully remote setting across multiple time zones.</li> <li>Highly organized with strong attention to detail and documentation accuracy.</li> <li>Proficient in Microsoft Office Suite and remote communication platforms (Zoom, Teams, etc.).</li> </ul> <p>Preferred Qualifications:</p> <ul> <li>Associate or Bachelor’s degree in health sciences or related field.</li> <li>Clinical research certification (e.g., ACRP, SoCRA).</li> <li>Prior experience supporting multi-site trials remotely.</li> <li>Bilingual proficiency is a plus.</li> </ul> <p>Work Schedule:</p> <p>Full-time (Remote), U.S. time zones (EST to PST)</p> <p>Perks of Working with UniTriTeam:</p> <ul> <li>Work with a mission-driven organization transforming the clinical research industry.</li> <li>Fully remote work environment with global team collaboration.</li> <li>Exposure to innovative research sites and a wide variety of protocols.</li> <li>Professional development and growth opportunities.</li> <li>Supportive and inclusive team culture.</li> </ul> </div> </div> </div> </div> <p><strong>Why Join Us?</strong><br>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:</p> <ul> <li>A collaborative and supportive work environment</li> <li>Opportunities for professional growth and advancement</li> <li>A chance to be part of meaningful research initiatives that change lives</li> </ul>