Clinical Research Coordinator: Impactful On-Campus Growth

Mayo Clinic; Rochester (MN); In loco; USD 60.000 - 80.000; Tempo pieno

Descrizione del lavoro

Mayo Clinic is seeking a Clinical Research Coordinator to support diverse research protocols on campus in Rochester, MN. The role involves coordinating interventional studies, collaborating with care teams, and ensuring regulatory compliance across activities.

You will screen and enroll participants, manage study data, and monitor study progress while maintaining high ethical and quality standards. Multiple schedules and shifts are available to fit candidate preferences and campus needs.

Mansioni

• Independently coordinate 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.
• 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.
• Participate in other protocol development activities and other assignments as assigned.
• Actively partner with team members by fostering an inclusive work environment and respecting others with different backgrounds, experiences and perspectives.

Conoscenze

Regulatory compliance

Clinical research coordination

Participant recruitment

Data management

Team collaboration

Descrizione del lavoro

Mayo Clinic is seeking a Clinical Research Coordinator to support diverse research protocols on campus in Rochester, MN. The role involves coordinating interventional studies, collaborating with care teams, and ensuring regulatory compliance across activities.

You will screen and enroll participants, manage study data, and monitor study progress while maintaining high ethical and quality standards. Multiple schedules and shifts are available to fit candidate preferences and campus needs.