UniTriTeam
Clinical Research
RemoteClinicalResearchCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Remote Clinical Research Coordinator at UniTriTeam. Skills: Clinical trial operations, Remote patient visits, Data management. Coordinate clinical trial operations remotely. Ensure compliance with study protocols”
Industry & Context.
Work across multiple time zones
What They're Looking For.
Must Have
2+ years clinical research coordination, 2+ years clinical operations, GCP understanding, ICH understanding, FDA regulatory requirements understanding, Fluent in English, Highly organized, Attention to detail, Documentation accuracy, Proficient in Microsoft Office Suite, Proficient in remote communication platforms
Nice to Have
Associate degree in health sciences, Bachelor's degree in health sciences, Clinical research certification, Prior experience supporting multi-site trials remotely, Bilingual proficiency
What You'll Do.
Coordinate clinical trial operations remotely
Ensure compliance with study protocols
Ensure compliance with regulatory guidelines
Support remote patient visits
Facilitate remote patient visits
Schedule remote patient visits
Document remote patient visits
Follow-up on remote patient visits
Support patient recruitment
Understand inclusion/exclusion criteria
Qualify patients for studies via phone
Maintain accurate data entry
Maintain timely data entry
Manage query resolution
Assist with regulatory document management
Assist with remote IRB submissions
Assist with remote IRB updates
Prepare for remote sponsor visits
Prepare for remote CRO visits
Prepare for remote monitoring visits
Prepare for remote audits
Prepare for remote inspections
Participate in remote sponsor visits
Participate in remote CRO visits
Participate in remote monitoring visits
Participate in remote audits
Participate in remote inspections
Serve as virtual liaison with sponsors
Serve as virtual liaison with CROs
Serve as virtual liaison with internal site teams
Support study startup tasks
Support study closeout tasks
Collect essential documents remotely
Verify essential documents remotely
Monitor visit schedules
Ensure subject documentation is complete
Ensure subject documentation is up to date
How You'll Work.
Team & Collaboration
Virtual liaison with sponsors; Virtual liaison with CROs; Virtual liaison with site teams; Global team collaboration
Communication Scope
Verbal communication; Written communication
Full Job Description
Remote Clinical Research Coordinator (Remote – PST/CST/EST Hours) LOCATION: Argentina 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 Englis
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