Clinical Trials Reporting Program Coordinator, CRMO - Georgetown University Medical Center

Location
Washington D.C
Posted
Jun 14, 2019
Closes
Jul 04, 2019
Ref
JR06826
Industry
Education
Hours
Full Time
Located in a historic neighborhood in the nation's capital, Georgetown offers rigorous academic programs, a global perspective, exciting ways to take advantage of Washington, D.C., and a commitment to social justice. Our community is a tight knit group of remarkable individuals interested in intellectual inquiry and making a difference in the world.

Requirements

Clinical Trials Reporting Program Coordinator, Clinical Research Management Office - GUMC

The Clinical Trials Reporting Program Coordinator (CTRPC) for the Clinical Research Management Office (CRMO) and Clinicaltrials.gov Coordinator works under general direction of CRMO Administrative Director to manage the various activities of registry and results data management for the National Cancer Institute (NCI) Clinical Trials Reporting Program (CTRP) and clinicaltrials.gov registrations. Duties include but are not limited to:
  • Manages the daily activities of the NCI Clinical Trials Reporting Program (CTRP).
  • Works closely with CRMO regulatory associates to ensure timely registration on clinicaltirals.gov website and with research coordinators to ensure timely and accurate patients registration in OnCore.
  • Works with various sites on investigator-sponsored trials where Lombardi is coordinating center to confirm patient's accrual and enter those accruals in OnCore and registers those trials and accruals in CTRP website.
  • Performs quality checks in OnCore to ensure accuracy of entered data, runs reports from OnCore and assists with preparation of reports as needed for the annual progress reports and the Cancer Center Support Grant renewal.
  • Assist CRMO Administrative Director and provide various reports for Cancer Center leadership.
  • Other relevant duties and responsibilities as assigned.


Qualifications
  • Bachelor's degree (preferably in science or related area).
  • Excellent intrapersonal and communication skills.
  • Detail oriented Excellent organization, planning and judgment skills. Self-starter.
  • Ability to work well with others.
  • Problem solving and conceptual skills.
  • Creative and independent thinking.
  • Understanding of medical terminology is a plus.
  • Knowledge of computer software, web design, structured query language (SQL), and databases.
  • Microsoft Office proficiency.
  • Ability to learn new programs and electronic information systems.


Preferred qualification
  • Master's degree (preferably in science or related area)
  • Experience working with databases and clinical trials data ;experience in a clinical research operations or research regulatory environment

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