Clinical Research Coordinator - Physical Medicine Rehabilitation

Mayo Clinic; Rochester (MN); Vor Ort; USD 52.000 - 72.000; Teilzeit

Zusammenfassung

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.

Qualifikationen

• Experience coordinating complex clinical research protocols.

Aufgaben

• 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.

Jobbeschreibung

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.

Please note this position is a 0.80 FTE (64 hours per pay period or every two weeks).

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