Mayo Clinic Healthcare London · 6 hours ago
Clinical Research Coordinator - Critical Care - Day/Evening
Rochester, MN, United States
Full-time
Onsite
Mid Level
$27.44/hr - $41.16/hr
3+ years expMayo Clinic Healthcare London is a renowned healthcare organization, and they are seeking a Clinical Research Coordinator for their Critical Care department. This role involves coordinating complex clinical research protocols, managing research activities, and ensuring compliance with regulatory laws and institutional guidelines.
Hospital & Health Care
No H1B
Responsibilities
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
Qualification
Required
HS Diploma with at least 5 years of clinical research coordination/related experience OR
Associate's degree/college Diploma/Certificate Program with at least 3 years of experience OR
Associate's in Clinical Research from an accredited academic institution without experience OR
Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience
Experience should be in the clinical setting or related experience
Preferred
Graduate or diploma from a study coordinator training program is preferred
One year of clinical research experience is preferred
Medical terminology course is preferred
Benefits
Medical: Multiple plan options.
Dental: Delta Dental or reimbursement account for flexible coverage.
Vision: Affordable plan with national network.
Pre-Tax Savings: HSA and FSAs for eligible expenses.
Retirement: Competitive retirement package to secure your future.
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