Remote Clinical Research Coordinator
New
U
UniTriTeamClinical Research
Location: Bogota, Colombia, EST to PSTFull-TimeMiddle
Salary not disclosed
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Job Details
- Languages
- English
- Experience
- 2+ years of experience in clinical research coordination or clinical operations
- Required Skills
- GCPData entry
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.)
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.
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