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Data Coordinator - Cardiology

Job in New York City, Richmond County, New York, 10261, USA
Listing for: Columbia University Irving Medical Center
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 64350 - 66350 USD Yearly USD 64350.00 66350.00 YEAR
Job Description & How to Apply Below

Position Summary

The Data Coordinator plays an integral role in managing and maintaining database systems within the Division of Cardiology, under the supervision of the Associate Director and Principal Investigator. The incumbent will work closely with the study team to support day-to-day data collection and management for clinical and research patients. This position is vital to ensuring data accuracy, regulatory compliance, and the timely completion of research milestones.

Responsibilities may expand in alignment with the growth of the division’s research portfolio.

Job Details
  • Salary Range: $64,350 - $66,350 annual
  • Grade: 103
  • Job Type: Officer of Administration
  • Regular/Temporary:
    Regular
  • Hours Per Week: 35
Responsibilities
  • Collaborate with Principal Investigators, treating physicians, and research nurses to attend clinical appointments and collect patient data.
  • Review study protocols to ensure appropriate data collection and management processes.
  • Review data at each clinical and/or research visit to confirm database completeness.
  • Reconcile data queries and resolve discrepancies.
  • Perform retrospective and prospective data entry for clinical and/or research patients.
  • Ensure accuracy, completeness, and contemporaneous entry of data to maintain up-to-date databases.
  • Conduct protocol-specific consenting processes.
  • Collect, process, store, and ship participant specimens in accordance with study protocols.
  • Prepare for and conduct study visits.
  • Maintain accountability for protocol-required supplies.
  • Complete required regulatory tasks and documentation.
  • Attend protocol-specific meetings and conferences.
  • Communicate effectively with study participants, clinicians, healthcare providers, ancillary staff, sponsors, and research office staff.
  • Complete and maintain all required institutional, protocol-related, and sponsor/vendor trainings, including Good Clinical Practice (GCP), Human Subjects Protection, and Clinical Research Coordinator course.
  • Prepare and maintain study source documents for inspections, audits, and monitoring visits.
  • Maintain accurate and organized electronic and hard‑copy files.
  • Perform additional duties as assigned.
Minimum Qualifications
  • Bachelor's degree or equivalent in training, education, and/or experience.
Preferred Qualifications
  • At least two years of related experience.
  • Advanced knowledge of medical terminology.
  • Spanish language proficiency.
Other Requirements
  • Knowledge of medical terminology and laboratory measures.
  • Strong attention to detail and familiarity with basic statistics.
  • Demonstrated ability to multi‑task, learn quickly, and operate efficiently.
  • Proven ability to take initiative and work independently with minimal supervision.
  • Ability to interact effectively with diverse constituencies, exercising tact and discretion.
  • Strong written communication skills with compassion, discretion, and follow‑through.
  • Proficiency in MS Word, Excel, PowerPoint, and Adobe.
  • Participation in the medical surveillance program.
  • Successful completion of applicable compliance and systems training requirements.
Equal Opportunity Statement

Equal Opportunity Employer / Disability / Veteran. Columbia University is committed to the hiring of qualified local residents.

Seniority Level
  • Entry level
Employment Type
  • Full‑time
Job Function
  • Information Technology
  • Hospitals and Health Care
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