Clinical Research Coordinator III

4 days ago


GondrecourtleChâteau, Grand Est, United States University of Minnesota Full time
About the Job

The University of Minnesota is seeking a highly skilled Clinical Research Coordinator III to join our team. As a key member of our research team, you will be responsible for providing technical expertise and overall management of clinical research data collection, study documentation, protocol-required procedure execution, and collaboration with PI and study team to ensure consistent and accurate implementation of the protocol.

Responsibilities
  • Interprets protocols and creates source documents needed for clinical research study
  • Identifies and reports protocol deviations within the required timeline in accordance with institutional requirements
  • Ensures protocol adherence by communicating and ensuring study parameters are executed according to protocol
  • Oversees visits with outside sponsors, including site initiation visits, interim monitoring visits and closeout visits
  • Collaborates with PI and study team to enroll study participants, execute study-required procedures, and maintain accurate source documentation
  • Maintains a processing and tracking system for protocol-required biospecimens, data, and procedures
  • Works as a member of the study team with positive and timely written and verbal communication, including sharing information up, down, and laterally
  • Troubleshoots problems in the development and implementation of protocol procedures
  • Coordinates with Investigational Drug Services (IDS), BioNet, clinical staff, and other bodies across campus to deliver drug, collect biospecimens, and execute the study visits according to protocol
Requirements
  • BA/BS with at least 4 years of experiences or an advanced degree and 2 years of experience or 8 years of relevant education & healthcare or research experience
  • Oncology experience in a clinical or research setting
  • Excellent attention to detail and organizational skills
  • Ability to work independently, as part of a team, and with changing priorities
  • Computer proficiency in a PC environment including Microsoft Office products
  • Ability to sit for extended periods of time
Preferred Qualifications
  • Clinical Research Coordinator certification or equivalent
  • Experience with disease-specific research or clinical care
  • Experience with patient contact / care
  • Experience abstracting clinical data and familiarity with medical terminology
  • Experience with Epic, Oncore, or equivalent medical record / Clinical Trial Management Systems


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