Clinical Research Coordinator - Cardiology

Columbia University Irving Medical Center; New York (NY); On-site; USD 64,000 - 75,000; Full time

Job summary

Columbia University Irving Medical Center is seeking a Clinical Research Coordinator for their Cardiovascular Research Lab. This role involves coordinating clinical trials, ensuring compliance, and managing participant data. Ideal candidates will possess strong communication skills, attention to detail, and a Bachelor's degree.

Qualifications

• Minimum two years of related experience.
• Demonstrated ability to multi-task and operate efficiently.
• Excellent written communication and compassion.

Responsibilities

• Coordinate management of clinical trial participants and tasks.
• Maintain compliance with relevant policies and regulations.
• Assist in regulatory tasks and data collection management.

Skills

Attention to detail

Communication skills

Phlebotomy

Education

Bachelor's degree or equivalent

Tools

MS Word

Excel

PowerPoint

Adobe

Job description

Clinical Research Coordinator - Cardiology

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

Clinical Research Coordinator - Cardiology

Join to apply for the Clinical Research Coordinator - Cardiology 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: $64,500 - $74,674 Annual
  
  

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

Under the direction and supervision of the Principal Investigator and Director, the Clinical Research Coordinator will play a key role in start-up, maintenance and closeout of protocols for the Clinical Cardiovascular Research Lab for the Elderly. Additionally, the Clinical Research Coordinator will be responsible of screening, recruitment and follow up of clinical trials participants.

Responsibilities

• Provide assistance for specified regulatory tasks.
• Maintain compliance with existing policies and procedures at Columbia University, the IRB, FDA, NIH, and NYPH that relate to clinical research.
• Participate in pre-study, initiation, monitor and close out visits.
• Recruitment and coordination of the clinical trial participants covering informed consent, screening, and inclusion of the subjects adhering to safety and compliance issues.
• Coordination and management of the clinical trial, communication with sponsor and monitors, visit coordination, sample acquisition and processing.
• Data collection and management, collection of source documents, registration, and management of AEs, filing and archiving, managing monitoring visits and managing queries.
• Coordinate Research Network related activities including telephone and in-person meetings.
• Serve as the resource for detailed information on assigned protocols and other investigational research activities.
• Attend conferences regarding clinical trials and disseminate information to clinical staff.
• Clearly and effectively communicate with study subjects, clinicians, and other health care providers, ancillary staff, sponsors, and research office staff.
• Maintain electronic and hard copy files.
• Perform other responsibilities as needed.
  
  

Minimum Qualifications

• Bachelor's degree or equivalent in training, education and/or experience.
• A minimum of two years related experience.
  
  

Preferred Qualifications

• The ideal candidate will show a demonstrated ability to multi-task, operate efficiently, learn and adapt quickly.
• High level of attention to detail and knowledge of basic statistics.
• Demonstrated ability to take initiative and able to work independently with minimal supervision.
• Ability to work with a wide range of constituencies, and exercise tact and discretion when interacting with faculty, administrators and students.
• Communication skills include excellent written communication skills, compassion, discretion, and follow-through.
• Phlebotomy experience.
• Proficiency in MS Word, Excel, PowerPoint, Adobe.
• Knowledge of medical terminology.
  
  

Other Requirements

• Must successful complete compliance and systems training requirements.
• Participation in Medical Surveillance Program:
• Contact with patients and/or human research subjects
• Potential bloodborne pathogen exposure
  

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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