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Clinical Research Coordinator

Minneapolis Clinic of Neurology
  • US
    Burnsville, Minnesota, United States
  • US
    Burnsville, Minnesota, United States

Über

Description
Perform pre-study duties necessary to start a clinical trial.
  • Understand the purpose, safety, confidentiality, benefits, and risks of clinical research trials.
  • Assess protocol for site operational feasibility and advise on site budgetary requirements.
  • Prepare for and conduct pre-study (site selection) and initiation visits.
  • Coordinate investigational staff and other disciplines (MRI, EKG, Lab, etc.) involved in studies.
  • Complete and submit the required regulatory documents to the IRB.
  • Maintain verbal and written communication with Institutional Review Boards.
  • Communicate study protocols to relevant hospital staff.
  • Develop and complete documentation in compliance with research protocol.
  • Screen and recruit patients for clinical research trials.

Manage multiple ongoing clinical trials.
  • Assure adherence to study-specific requirements.
  • Organize receipt, storage and return of study supplies, including study drug, and maintain accurate accountability logs as appropriate.
  • Schedule and conduct patient appointments as required by research protocol.
  • Obtain medical status, including histories, from potential and current study patients as appropriate.
  • Abstract relevant study information from patients' medical records.
  • Obtain and document patients' blood pressure, weight and height.
  • Perform clinical laboratory and EKG services as required by the research protocol.
  • Report abnormal laboratory and EKG results to the Principal Investigator.
  • Develop, complete, and collect documentation in compliance with research protocol.
  • Coordinate investigational staff and other disciplines (e.g. MRI, EKG, Lab) involved in studies.
  • Provide education to patients under physicians' direction and assure his/her understanding.
  • Complete and submit the required regulatory documents and emergent serious medical events to the IRB under direction of Principal Investigator.
  • Meet with study monitors and assure query resolution as necessary or requested.
  • Assure financial reconciliation against contract, including timely and accurate
  • Burnsville, Minnesota, United States

Sprachkenntnisse

  • English
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