UniTriTeam

Clinical Research

RemoteClinicalResearchCoordinator

$10000–15000k ~AI est. Argentina; United States FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“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.

Clinical Research
Eligibility Requirements

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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