Hybrid Clinical Research Coordinator - Protocols & Data

Mayo Career Site UK; Rochester (MN); Hybrid; USD 52,000 - 75,000; Full time

Job summary

Mayo Clinic in Rochester, MN seeks a Clinical Research Coordinator to independently coordinate complex interventional protocols, ensure IRB approval compliance, screen and enroll participants, and manage data to maintain quality and regulatory standards.

The role collaborates with the research team, provides training, and handles protocol development activities, with potential hybrid work once settled near the Rochester campus; visa sponsorship is not available.

Responsibilities

• Independently coordinate complex clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
• Collaborate with research team to assess feasibility and management of research protocols.
• Screen, enroll, and recruit research participants.
• Coordinate schedules and monitor research activities and subject participation.
• Identify, review, and report adverse events, protocol deviations, and other unanticipated problems appropriately.
• Manage, monitor, and report research data to maintain quality and compliance.
• Provide education/training for others within the department.
• Perform administrative and regulatory duties related to the study as appropriate.

Job description

Mayo Clinic in Rochester, MN seeks a Clinical Research Coordinator to independently coordinate complex interventional protocols, ensure IRB approval compliance, screen and enroll participants, and manage data to maintain quality and regulatory standards.

The role collaborates with the research team, provides training, and handles protocol development activities, with potential hybrid work once settled near the Rochester campus; visa sponsorship is not available.