Clinical Research Coordinator – Endocrinology

Details

Posted: 13-Feb-24

Location: New York, New York

Type: Full-time

Salary: Open

Categories:

Staff/Administrative

Internal Number: 541839

• Job Type: Officer of Administration
• Regular/Temporary: Regular
• Hours Per Week: 35
• Salary Range: $58,500 – $62,000

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

Clinical Research Coordinator (CRC) is sought to assist with recruitment, assessment, follow-up and the conduct of a NIH multicenter clinical trial. Candidate must be a motivated self-starter with the ability to exercise independent judgement within the scope of the research in order to meet expected goals. Reporting to the Program Administrator and the Principal Investigators, the CRC will work with other research staff, collect data, and communicate with a data coordinating center. 

Responsibilities

• Assist with the conduct and coordination of a clinical trial including recruitment of participants, assessment, data collection, and follow-up.
• Provide patient education regarding study procedures, logistics, and inclusion/exclusion criteria.
• Schedule and organize study visits and perform follow up visits.
• Obtain informed consent and administer standardized questionnaires.
• Review and extract data from patient charts.
• Maintain patient registry and provide recruitment reports.
• Ensure compliance with study protocol.
• Responsible for data entry and maintenance of database.
• Monitor safety data and maintain case report forms.
• Responsible for preparation of documents for renewals, modification, yearly submissions, correspondence, and audit related to the Institutional Review Board (IRB).
• Assist with preparation of data for statistician.
• Develop ongoing reports for the PI, statistician, and sponsor.
• Perform other related duties as assigned.

Minimum Qualifications

• Bachelor’s degree or equivalent in education, training and experience
• Computer skills including Word, Excel
• Strong interpersonal communication skills
• Experience with patients and/or human subjects
• Excellent verbal and written communication skills
• Attention to detail

Preferred Qualifications

• Experience in administration of clinical trials
• Phlebotomy certification
• Spanish language skills

Other Requirements

• Participation in medical surveillance program
• Contact with patients and/or human research 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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About Columbia University
Columbia University is one of the world’s most important centers of research and at the same time a distinctive and distinguished learning environment for undergraduates and graduate students in many scholarly and professional fields. The University recognizes the importance of its location in New York City and seeks to link its research and teaching to the vast resources of a great metropolis. It seeks to attract a diverse and international faculty and student body, to support research and teaching on global issues, and to create academic relationships with many countries and regions. It expects all areas of the university to advance knowledge and learning at the highest level and to convey the products of its efforts to the world.
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