Travel Clinical Research Coordinator I - Remote

Overview

The Travel Clinical Research Coordinator I is responsible for overseeing clinical studies, ensuring compliance with protocols and regulations, and managing patient interactions and data documentation.

In Short

• 100% travel required within the US.
• Works under the supervision of the Principal Investigator and site personnel.
• Maintains documentation associated with clinical studies.
• Ensures compliance with FDA, GCP, and ICH guidelines.
• Identifies potential study participants and obtains informed consent.
• Schedules patient visits and prepares necessary labs/tests.
• Monitors patients' conditions and documents observations.
• Conducts ongoing assessments of study execution.
• Prepares and submits regulatory documents.
• Maintains study records according to GCP.

Requirements

• Bachelor’s Degree or equivalent in healthcare.
• 2 to 5 years of healthcare experience, preferably with dialysis.
• Research experience highly preferred.
• Proficient with PCs and Microsoft Office applications.
• Good communication and organizational skills.
• Ability to work independently.
• Current appropriate state licensure if applicable.
• Willing to pursue CCRC or SoCRA certification.

Benefits

• Opportunity to work in a dynamic healthcare environment.
• Support for professional development and certification.
• Engagement in meaningful clinical research.
• Collaboration with a team of dedicated professionals.
• Flexible work environment with travel opportunities.