Remote Clinical Research Coordinator

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IndeedClinical Research
Location: Mexico City. Mexico, PST/EST/CSTFull-TimeMiddle
Salary not disclosed
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Job Details

Languages
Fluent in English – both verbal and written communication required.
Experience
2+ years
Required Skills
GCPMicrosoft Office Suite

Requirements

  • 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.).
  • Associate or Bachelor’s degree in health sciences or related field (preferred).
  • Clinical research certification (e.g., ACRP, SoCRA) (preferred).
  • Prior experience supporting multi-site trials remotely (preferred).
  • Bilingual proficiency is a plus (preferred).

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.
  • Perform 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.
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