To assist and support MDs and PhDs on their research and independently coordinate Phase I-III therapeutic and non-therapeutic adult and/or pediatric clinical research for local investigator initiated and pharmaceutical sponsored trials. A CRC ensures patient safety, protocol compliance and data integrity.
Maintain a current and working knowledge of gynecologic cancers and their relative standard of care treatment and clinical research.
Maintain a current knowledge and apply all recognized ICH Good Clinical Practice (GCP) Standards and Health Insurance Portability and Accountability Act (HIPAA) regulations to the conduct of CTO Clinical trials.
Independent Trial Management/Coordination as a Subject Coordinator 35%
Data Management 35%
Assist with study procedures under direction and collaboration with Nurse Coordinator as a Clinical Research Associate 15%
Administrative and Other 15%
***All required qualifications must be documented on application materials***
BA/BS in a scientific or health related field or a combination of relevant education and healthcare experience equal to 4 years.
Demonstrated knowledge of medical terminology.
Demonstrated ability to identify data for abstraction.
Working knowledge of Microsoft applications (Word, Access, Excel).
Excellent attention to detail and organizational skills.
Ability to work independently, as part of a team, and with changing priorities.
Ability to sit for long periods of time.
Strong clinical background
Relevant experience with data management
Experience with patient care/contact
Familiarity with University of Minnesota, UMN Medical Center and Fairview hospitals
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.