UniTriTeam

Clinical Research

RemoteClinicalResearchCoordinator

$11000–17000k ~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 research coordination, Remote patient visits, Clinical trial support. Coordinate day-to-day clinical trial operations. Ensure compliance with study protocols”

Industry & Context.

Clinical Research

What They're Looking For.

Must Have

2+ years of experience in clinical research coordination or clinical operations, understanding of GCP, ICH, and FDA regulatory requirements, Fluent in English – both verbal and written communication required, Comfortable working independently in a fully remote setting across multiple time zones, Highly organized with attention to detail and documentation accuracy

Nice to Have

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

What You'll Do.

Coordinate day-to-day clinical trial operations

Ensure compliance with study protocols

Ensure compliance with regulatory guidelines

Support remote patient visits

Facilitate remote patient visits

Maintain accurate data entry in EDC

Maintain timely data entry in EDC

Manage query resolution

Assist with regulatory document management

Assist with remote IRB submissions

Assist with remote IRB updates

Prepare for remote sponsor monitoring visits

Prepare for remote CRO monitoring visits

Prepare for remote audits

Prepare for remote inspections

Serve as a virtual liaison with sponsors

Serve as a virtual liaison with CROs

Serve as a virtual liaison with internal site

Support study startup tasks

Support study closeout tasks

Support remote collection of essential documents

Support remote verification of essential documents

Monitor visit schedules

Ensure all subject documentation is complete

Ensure all subject documentation is up to date

How You'll Work.

Team & Collaboration

Virtual liaison with sponsors; Virtual liaison with CROs; Virtual liaison with internal site teams; Global team collaboration

Communication Scope

Verbal communication; Written communication

Full Job Description

Remote Clinical Research Coordinator (Remote – PST/CST/EST Hours) LOCATION: India 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 –

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