Clinical Research Coordinator (Research Professional 2)
University of Minnesota, Twin Cities
Location: Minneapolis, Minnesota
Salary: 39499.20 - 68016.00
Internal Number: 341954
The Department of Radiation Oncology is seeking a Research Coordinator to provide research assistance in implementing, managing and coordinating research protocols and related study activities. The coordinator will ensure that all components of a project are completed in an ethical, scientific, rigorous, and timely manner. Duties are determined by protocol-specific requirements and may include any research activity from protocol development through study closeout.
Prepares and submits all protocol applications, amendments, continuing reviews, and informed consent documents for IRB review and approval.
Prepares, maintains and organizes regulatory files for each assigned study in compliance with study protocol or sponsor requirements.
Maintains regulatory binders and tracking databases with information related to study recruitment, subject enrollment, and study progress and completion.
Determines subject eligibility, screens, recruits, consents and enrolls potential subjects.
Collects and ships specimens for research, laboratory, or clinical testing as required.
Reviews data collection forms for completeness and accuracy, and abstracts data from medical records using standard forms.
Assists in drafting scientific communications including grant proposals, progress reports, presentations and scientific manuscripts.
Demonstrates effective and efficient communication with study investigators, collaborators, clinic personnel, sponsors, monitors, department and university staff.
Educates department faculty and staff on regulatory and research obligations in relation to clinical research activities.
Attends research and professional development trainings where appropriate.
All required qualifications must be documented on application materials.
Bachelor’s degree plus 2 years of related research experience, OR a combination of related education and work experience to equal 6 years.
Proficiency with Microsoft Office, Zoom and Google Suite.
Ability to work independently, problem solve, and prioritize the simultaneous management of multiple projects.
Strong organizational, communication and time management skills.
Experience working with clinical research, preferably at the University of Minnesota.
Certification as a Clinical Research Coordinator (CCRC, CCRP, or similar certification)
Experience providing oversight for grant proposals and budgets.
Experience with research database software (REDcap, OnCore, and Microsoft Access)
Experience with EPIC
Experience in database management, statistics, and writing of scientific reports
The University of Minnesota, founded in the belief that all people are enriched by understanding, is dedicated to the advancement of learning and the search for truth; to the sharing of this knowledge through education for a diverse community; and to the application of this knowledge to benefit the people of the state, the nation, and the world.