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Mayo Clinic · 3 weeks ago

Clinical Research Coordinator - Comprehensive Cancer Center

Rochester, MN, United States

Full-time

Hybrid

Mid Level

$27.44/hr - $41.16/hr

Mayo Clinic is a world-class healthcare institution, and they are seeking a Clinical Research Coordinator for their Comprehensive Cancer Center. The role involves independently coordinating complex clinical research protocols, collaborating with research teams, and ensuring compliance with regulatory standards.

BiotechnologyHealth CareHospitalMedicalWellness

No H1B

Responsibilities

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

Ensure implementation of research protocols after IRB approval and provide information as appropriate for progress reports

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

Perform Protocol Development and Maintenance Activities Responsibilities, which 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 apply 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

Participate in other protocol development activities and execute other assignments as warranted and assigned

*Some travel may be required

Qualification

Clinical research coordinationRegulatory complianceProtocol developmentData managementParticipant recruitmentAdverse event reportingTeam collaboration