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Clinical Research Coordinator - Endocrinology


Clinical Research Coordinator - Endocrinology

  • 530763
  • Medical Center
  • Medicine
  • Full Time
  • Opening on: Dec 23 2022
  • Grade 103
  • Job Type: Officer of Administration
  • Bargaining Unit: n/a
  • Regular/Temporary: Regular
  • End Date if Temporary: n/a
  • Hours Per Week: 35
  • Salary Range: Commensurate with experience

Position Summary

Working closely with the Principal Investigator, the Clinical Research Coordinator will assist in all aspects of human physiologic studies in the field of type 2 diabetes and non-alcoholic fatty liver disease.

We are seeking a Clinical Research Coordinator to assist in all aspects of human physiologic studies in the field of type 2 diabetes and non-alcoholic fatty liver disease. The CRC will work closely with the Principal Investigator to assist in the coordination of tests/visits for research participants, interface with vendors and collaborating services, ensure regulatory compliance, and curate and enter study data. The Candidate should be motivated, excited to play a crucial role in research, and willing to exercise independent judgment within the scope of the research in order to meet expected goals.

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  • Assist with the day-to-day general operation of clinical research projects.
  • Screen participants, recruit/retain participants, and schedule and organize study visits.
  • Assist with the conduct of study procedures.
  • Educate participants regarding study procedures, logistics, and other pertinent information.
  • Coordinate reimbursements/compensation for study participants.
  • Coordinate of tests/visits for research participants.
  • Responsible for data collection and entry; maintain study database, and ensure data accuracy.
  • Monitor data (including safety data) on case report forms.
  • Ensure compliance with the study protocol and all relevant research regulations.
  • Interact with centralized research resources such as the Institutional Review Board (IRB), the Clinical Research Center (CTSA-CRR), the Clinical Trials Office (CTO), and other regulatory bodies.
  • Responsible for inventory and procurement of supplies, including contact with vendors, proper storage, and keeping up-to-date logs.
  • Assist with publications, various grant reports, and agency reporting including NIH Data Safety Monitoring: generate graphs, figures, tables, and organize references with EndNote.
  • Perform additional related duties as needed.

Minimum Qualifications

  • Bachelor’s degree or equivalent in education, training, and experience, plus two years of related experience
  • Basic computer skills including Microsoft Office
  • Strong verbal and written communication skills
  • Careful attention to detail
  • Ability to work independently, developing and exercising professional judgment, and thinking creatively to work through problems
  • Excited to engage in all aspects of scientific research involving human participants

Preferred Qualifications

  • Proficiency in Spanish and/or willingness to use phone interpreter service
  • Prior experience working with patients and/or human participants under HIPAA and GCP
  • Working knowledge of electronic research tools such as Epic (electronic health record) and/or Clinical Trial Management Systems

Other Requirements

  • Participation in the medical surveillance program
    • Potential bloodborne pathogen exposure
    • Contact with patients and/or human research participants
  • Successful completion of applicable compliance and systems training requirements

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residents.

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