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Clinical Research Coordinator - PACC

Job in New York, New York County, New York, 10261, USA
Listing for: Columbia University Irving Medical Center
Full Time position
Listed on 2026-01-02
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 64350 - 70000 USD Yearly USD 64350.00 70000.00 YEAR
Job Description & How to Apply Below
Location: New York

Join to apply for the Clinical Research Coordinator - PACC role at Columbia University Irving Medical Center

Join to apply for the Clinical Research Coordinator - PACC role at Columbia University Irving Medical Center

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Grade 103

  • Job Type: Officer of Administration
  • Regular/Temporary:
    Regular
  • Hours Per Week: 35
  • Salary Range: $64,350.00 - $70,000.00
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 Clinical Research Coordinator for the Columbia University Irving Medical Center Lung Transplant Program will facilitate the screening, enrollment, and treatment of research subjects for our ongoing clinical research projects.

Responsibilities

  • Manage study participants by facilitating screening, enrollment, and treatment in compliance with regulatory requirements, study protocols, and internal standard operating procedures.
  • Perform protocol-specific activities, including but not limited to recruiting and consenting patients, conducting study visits, coordinating specimen collection, processing and shipping samples, and maintaining accurate source documentation and data entry.
  • Collect, record, and accurately input study data into electronic data capture (EDC) systems.
  • Assist in eligibility assessments and obtaining written informed consent, as appropriate.
  • Facilitate sample collection, processing, and storage activities.
  • Support regulatory submissions, including protocol reviews and monitoring processes.
  • Communicate effectively with clinical staff, study sponsors, patients, and other members of the research team.
  • Assist with short-term projects and provide cross-coverage for other research team members as needed.


Minimum Qualifications

  • Bachelor's degree or equivalent in education, training, and experience.


Preferred Qualifications

  • At least one year of experience in a clinical research setting.
  • Bilingual proficiency in both English and Spanish.
  • Familiarity with electronic medical record platforms (e.g., Epic) and electronic data capture systems (e.g., REDCap).
Other Requirements
  • Medical clearance and participation in the medical surveillance program
    • Contact with patients and/or human research subjects
  • 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.

Seniority level
  • Seniority level

    Entry level
Employment type
  • Employment type

    Full-time
Job function
  • Job function

    Research, Analyst, and Information Technology
  • Industries Hospitals and Health Care

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