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

Indeed; United States; Remote; USD 65,000 - 90,000; Full time

Benefits offered by this job

Mission-driven org

Fully remote

Diverse protocols

Professional development

Inclusive culture

Job summary

UniTriTeam is seeking a Remote Clinical Research Coordinator to support one of our clinical research site clients. This fully remote role involves coordinating remote patient visits and behind-the-scenes trial support across multiple time zones.

The ideal candidate has experience with GCP/ICH/FDA guidelines, CTMS platforms like CRIO or Clinical Conductor, and strong English communication. A detail-oriented, independent worker will thrive in a global, mission-driven team.

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.).

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.

Skills

GCP & ICH & FDA

CTMS CRIO/Clinical Conductor

English fluency

Remote work capability

Strong organizational skills

MS Office & collaboration tools

Education

Associate or Bachelor’s degree in health sciences

Tools

CRIO

Clinical Conductor

Microsoft Office

Zoom

Teams

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 – 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