utt logo

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

utt

Buenos Aires, Argentinafull-timePosted 0 day(s) ago$0-$0 / yr

$0-$0 / yr

Salary

buenos aires, argentina

Region

ASAP

Start Date

About utt

No company information provided.

About this Role.

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 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

Skills Required

Benefits & Perks

Ready to Apply?

Apply Now

Similar jobs

No similar jobs found.