Clinical Research Coordinator — Interventional Trials

Mayo Clinic; Rochester (MN); On-site; USD 52,000 - 72,000; Part time

Job summary

Mayo Clinic in Rochester, Minnesota seeks a clinical research professional to independently coordinate complex interventional studies with minimal supervision. You will ensure IRB approvals, monitor participant enrollment, and manage regulatory duties while collaborating with the research team to ensure protocol feasibility and compliance.

The role includes data management, adverse event reporting, and education of staff.

Qualifications

• Experience coordinating complex clinical research protocols.

Responsibilities

• Coordinate complex clinical research protocols with minimal direction from PI or supervisor in compliance with regulatory laws and guidelines.
• Collaborate with research team to assess feasibility and manage protocols.
• Screen, enroll, and recruit participants; coordinate schedules and monitor activities.
• Identify, review, and report adverse events and protocol deviations; maintain data quality and compliance.
• Provide education/training within the department; perform regulatory duties; travel may be required.
• Support protocol development and maintenance, including document management and site communications.

Job description

Mayo Clinic in Rochester, Minnesota seeks a clinical research professional to independently coordinate complex interventional studies with minimal supervision. You will ensure IRB approvals, monitor participant enrollment, and manage regulatory duties while collaborating with the research team to ensure protocol feasibility and compliance.

The role includes data management, adverse event reporting, and education of staff.