Senior Clinical Research Coordinator

4 weeks ago


Chicago, Illinois, United States The University of Chicago Full time
About the Role

The University of Chicago is seeking a highly skilled Senior Clinical Research Coordinator to join our team in the Department of Medicine. This is a specialized researcher position that will partner with the clinical Principal Investigator and under the direction of the Section Administrator and/or Clinical Research Manager within the Section of Pulmonary/Critical Care Medicine.

The Senior Clinical Research Coordinator will oversee, facilitate, and coordinate the daily activities of complex clinical trials and play a critical role in the conduct of the studies to ensure compliance with federal and institutional regulations.

Key Responsibilities
  • Leads within the department/unit through improving clinical research practice and serves as a resource to others.
  • Works with the PIs, department, sponsors, and institution to support and provide guidance on the administration of the compliance, financial, personnel, and other related aspects of the clinical studies.
  • Assists with or plans and implements the clinical study's goals and objectives; organizes patient enrollment planning; conducts quality assurance activities, compiles and analyzes data.
  • Acts as a liaison with medical staff, University departments, ancillary departments, and/or satellite facilities.
  • Serves as a resource person or acts as a consultant within the area of clinical expertise.
  • Maintains working knowledge of current protocols and internal SOPs.
  • Accountable for high standards of clinical research practice and assists in the development of accountability in others.
  • Develops and implements procedures, maintains records, tracks progress, and conducts quality assurance on data collected.
Requirements
  • Minimum requirements include a college or university degree in a related field.
  • Minimum requirements include knowledge and skills developed through 57 years of work experience in a related job discipline.
  • Certifications: Preferred Qualifications
  • Master's degree.
  • Clinical research experience coordinating multiple and variety of studies (e.g., investigator-initiated; industry-sponsored; multisite trials).


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