Clinical Research Coordinator - PACC

Columbia University Irving Medical Center; New York (NY); On-site; USD 64,350 - 70,000; Full time

Job summary

A prestigious medical institution in New York is seeking a Clinical Research Coordinator to manage clinical studies within its Lung Transplant Program. This entry-level role involves facilitating participant screening and enrollment, ensuring compliance with research protocols, and managing data entry. Candidates should have a Bachelor's degree and at least one year of clinical research experience. Bilingual proficiency in English and Spanish is preferred. This position offers a full-time contract and competitive salary.

Qualifications

• Bachelor's degree or equivalent in education, training, and experience.
• At least one year of experience in a clinical research setting.
• Bilingual proficiency in both English and Spanish.

Responsibilities

• Facilitate screening, enrollment, and treatment of research subjects.
• Manage study participants in compliance with protocols.
• Collect and input study data into electronic data capture systems.

Skills

Clinical research experience

Bilingual in English and Spanish

Knowledge of EDC systems

Education

Bachelor's degree or equivalent

Tools

Epic

REDCap

Job description

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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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