Job detail

Clinical Research Coordinator - Comprehensive Cancer Center

Mayo Clinic

#Medical Terminology #Clinical Setting #Clinical Research #Protocol Development #Data Quality #Cancer Center #Mayo Clinic #IRB #Regulatory Affairs

Quick overview

Independently coordinate complex clinical research protocols and manage the end-to-end process from IRB approval to data reporting. Responsibilities include screening and enrolling participants, monitoring research activities, and ensuring compliance with regulatory laws.

Requirements summary

Requires a high school diploma with 5 years of experience, an associate degree with 3 years, or a bachelor's degree with 1 year of clinical research experience. Preferred qualifications include a study coordinator training program certificate and knowledge of medical terminology.

high schoolassociate degreebachelor degreeprofessional certificateRegulatory ComplianceMedical TerminologyData ManagementProtocol DevelopmentPatient ScreeningClinical Research CoordinationAdverse Event ReportingParticipant RecruitmentProtocol ManagementIRB Compliance

Job description

Don't miss this chance to join a world-class team and make a difference in the lives of millions of patients. Apply today and become part of the Mayo Clinic Experience.

As a Clinical Research Coordinator, you will

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.

**This position may have the option of working hybrid after some time, requiring the candidate to be within 100 miles of the Rochester, MN campus.**

Clinical Research Coordinator - Comprehensive Cancer Center

Quick overview

Requirements summary

Job description

As a Clinical Research Coordinator, you will

Benefits

Why Mayo Clinic

Benefits

Equal Opportunity

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