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Clinical Research Coordinator (PST/EST/CST Timezone)

unitriteam

Bogota, Colombia; Buenos Aires, Argentina; Cairo, Egypt; DF, Mexicofull-timePosted 0 day(s) ago$0-$0 / yr

$0-$0 / yr

Salary

bogota, colombia; buenos aires, argentina; cairo, egypt; df, mexico

Region

ASAP

Start Date

About unitriteam

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About this Role.

**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

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