Mayo Clinic Healthcare London · 1 month ago
Clinical Research Coordinator - Comprehensive Cancer Center
Rochester, MN, United States
Full-time
Hybrid
Mid Level
$27.44/hr - $41.16/hrMayo Clinic Healthcare London is a leading healthcare provider, and they are seeking a Clinical Research Coordinator to manage complex clinical research protocols. The role involves coordinating research activities, ensuring compliance with regulatory laws, and collaborating with the research team to assess feasibility and manage protocols.
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
Qualification
Required
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
Preferred
Some travel may be required
This position may have the option of working hybrid after some time, requiring the candidate to be within reasonable driving distance of the Rochester, MN campus
Visa sponsorship is not available for this position
This position is not eligible for F-1 OPT STEM extension
Company
Mayo Clinic Healthcare London
Located in the Harley Street District in London, Mayo Clinic Healthcare offers an array of services, including Executive Health Assessments, GP Services, Outpatient Cardiology, Cardio-thoracic, Respiratory, Neurology and Neurosurgery, Colorectal, Gastroenterology, General Internal Medicine, Orthopaedic, Rheumatology and Endocrinology specialist consultations.
51-200 employees
Funding
Current Stage
Growth StageCompany data provided by crunchbase