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Clinical Research Coordinator - Endocrinology (NYORC)

  • 550192
  • Columbia University Medical Center
  • Medicine
  • Full Time
  • Opening on: Jun 4 2025
  • Grade 103
  • Job Type: Officer of Administration
  • Regular/Temporary: Regular
  • Hours Per Week: 35
  • Salary Range: $64,350 - $64,350
The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.

Position Summary

The New York Obesity Research Center in the Division of Endocrinology is seeking a Clinical Research Coordinator to assist the PI and the Clinical Research Manager in all aspects of clinical trials in the field of obesity and type 2 diabetes. The incumbent will assist in the coordination of tests/visits for research participants, and work with the study team to maximize work efficacy to gather all required data and relevant clinical information.


Responsibilities

  • Adhere to all Columbia University clinical research regulations, including COVID precautions.
  • Maintain extensive knowledge of all aspects of the protocol: inclusion/exclusion criteria, procedures, methods, data collection procedures, timeline, and outcome variables.
  • Assist in preparation of study related documentation for submission to the Institutional Review Board (IRB), the Clinical Research Center (CTSA-CRR), and the Clinical Trials Office (CTO).
  • Assist with the day-to-day general operation of clinical research projects including screening, recruiting and retaining research participants for obesity and diabetes prevention lifestyle studies.
  • Perform data acquisition, materials calibration and standardization of the study app, actigraphy and continuous glucose monitoring system.
  • Responsible for inventory and procurement of supplies including contact with vendors, proper storage, and keeping up-to-date logs.
  • Responsible for biospecimen processing, assay requests, and freezer maintenance.
  • Perform data entry in database and ensure data accuracy.
  • Assist with publications, various grant reports 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
  • Computer proficiency in MS Word and Excel

Preferred Qualifications

  • Master’s Degree in related field
  • Experience in a clinical research setting with knowledge of HIPAA, GCP and EPIC
  • Phlebotomy skills

Other Requirements

  • Participation in the medical surveillance program
    • Contact with patients and/or human subjects
    • Potential bloodborne pathogen exposure
  • 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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