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

External
utt logoUtt · Lima, Peru
Full-timeOn-site1mo ago
ComplianceDocumentationGCP
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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.

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.).

Requirements

  • 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

Benefits

Health insuranceRemote work options

Additional Information

Remote Clinical Research Coordinator (Remote - PST/CST/EST Hours) LOCATION: Peru 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.


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