Senior Clinical Research Coordinator
Job ID: R0030709 | Clinical Research | Full Time | Charlottesville, VA
The Division of Infectious Diseases at the University of Virginia seeks a senior Clinical Research Coordinator, licensed or non-licensed, to oversee IRB proposal submissions and annual reporting for multiple clinical research projects. Submit study protocols and amendments, consent forms and recruiting materials to the Institutional Review Board and department for approval with oversight from the supervisor.

Senior Clinical Research Coordinator plans, organizes, leads and performs comprehensive, advanced-level clinical trial duties for multiple and/or complex clinical trials, focusing on the overall productivity and success of the clinical trials. They perform some patient-related care and assessments independently and within the scope of their licensure. They work independently and have the authority to adapt methods and procedures to meet the needs of the clinical trial. They influence the long-term goals of clinical research trial and process. They often manage support staff or other clinical research coordinators. The incumbent's duties and responsibilities will include:
  • Overseeing quarterly review of all principal investigator accounts, performing a strategic analysis of PI research portfolios.
  • Compiling data and documents during internal and external audits and being ultimately responsible for quality of submissions.
  • May recruit, screen and enroll study participants who meet research criteria.
  • Collecting basic information through scripted interviews and answer general questions.
  • Obtaining informed consent from study participants and maintaining telephone and in-person contact.
  • Notifying principal investigator and supervisor of subject status.
  • Collecting subject data, entering and analyzing data, and compiling reports, adhering to proper research protocols.
  • Preparing documentation, reports, graphs and other materials.
  • Keeping appropriate logs, tracking participants and preparing study materials.
  • In addition to the above job responsibilities, other duties may be assigned.

  • Education: Associate's degree or higher based on medical specialty.
  • Experience: At least 4 years of clinical research experience. Related graduate degree may substitute for three years of experience.
  • Licensure: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is a plus.

This is primarily a sedentary job involving extensive use of desktop computers. The job does occasionally require traveling some distance to attend meetings and programs.

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Charlottesville, VA
Charlottesville, VA 22903

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