Clinical Research Coordinator - Alzheimer's Disease Research

Mayo Career Site US; Rochester (MN); On-site; USD 65,000 - 90,000; Full time

Job summary

The Mayo Clinic in Rochester, MN seeks a Clinical Research Coordinator who can independently coordinate complex protocols, ensure regulatory compliance, and collaborate with a research team to manage study logistics.

The role includes screening and enrolling participants, monitoring data quality, reporting adverse events, and supporting protocol development. Some travel may be required, and the position emphasizes adherence to IRB and federal standards.

Qualifications

• Coordinate complex clinical research protocols with minimal direction.
• Screen, enroll, and recruit research participants.
• Some travel may be required.
• Comply with IRB and federal regulations.

Responsibilities

• Coordinate protocol development and maintenance activities.
• Manage study logistics and data collection.
• Provide education/training within the department.
• Prepare regulatory documents and reports.

Skills

Cognitive testing

Clinical research coordination

Job description

Independently coordinates complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. Collaborates with research team to assess feasibility and management of research protocols. Ensures implementation of research protocols after IRB approval and provides information as appropriate for progress reports. Screens, enrolls, and recruits research participants. Coordinates schedules and monitors research activities and subject participation. Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately. Manages, monitors, and reports research data to maintain quality and compliance. Provides education/training for others within the department. Performs administrative and regulatory duties related to the study as appropriate. Some travel may be required. Protocol Development and Maintenance Activities Responsibilities may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. blood collection kits, data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; communication with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements. Accurately applies investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements. Participates in other protocol development activities and executes other assignments as warranted and assigned.

Cognitive testing is a required part of this position. Applicants do not need prior experience but should be comfortable learning to administer standardized cognitive assessments as part of their regular responsibilities.

*Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.