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    Clinical Research Coordinator - New Orleans, United States - Tulane University

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    Summary

    Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future Oncology research projects. Responsible for data collection, management, and compliance with federal and IRB regulatory policies.

    Required Knowledge, Skills, and Abilities
  • Excellent written and verbal communication
  • Excellent computer literacy skills, including knowledge of standard office software
  • Required Education and/or Experience
  • Bachelor's Degree or RN with current LA licensure at the time of hire
  • Two years clinical research experience
  • Preferred Qualifications
  • Master's degree in Public Health, Business or Social work preferred
  • Compensation Information This position is classified as "non-exempt, hourly" and is assigned to pay grade 25. Tulane offers a variety of options to enhance your health and well-being so that you may enjoy more out of life now and in the future. Learn more about as well as our Benefits and Pay. See our Candidate Resources to learn more about our hiring process and what to expect.


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