About the Role
The Clinical Research Coordinator will manage trial-related activities, ensure adherence to protocols, coordinate with research sites, and maintain accurate documentation throughout the study lifecycle.
Responsibilities
- Coordinate daily operations of clinical trials across multiple sites
- Ensure compliance with regulatory standards and internal procedures
- Schedule and support site initiation, monitoring, and closeout visits
- Review case report forms for completeness and accuracy
- Communicate regularly with site personnel to resolve issues
- Maintain essential regulatory documents in trial master files
- Assist in preparing for audits and inspections
- Track trial milestones and report progress to project leads
- Verify informed consent processes meet ethical requirements
- Support investigator recruitment and retention efforts
- Organize trial-related training for site staff
- Monitor data entry timelines and follow up on delays
- Coordinate shipment and accountability of investigational products
- Update trial databases with current site status information
- Participate in protocol development and feasibility assessments
- Serve as primary point of contact for assigned sites
- Document trial communications and deviations appropriately
- Ensure adverse events are reported per protocol guidelines
- Collaborate with cross-functional teams on study execution
- Maintain up-to-date knowledge of clinical research regulations
Compensation
Competitive salary and benefits package
Work Arrangement
Remote with flexible hours within PST/EST/CST time zones
Team
Collaborative team environment focused on clinical trial execution
Time Zone Requirement
Applicants must reside in and be able to work during PST, EST, or CST business hours
Work Environment
- Fully remote position with asynchronous collaboration using digital tools
- Regular virtual meetings scheduled within common time zones
Not available
