Clinical Research Coordinator II - Study Oversight

Columbia University Irving Medical Center; New York (NY); On-site; USD 75,000 - 85,000; Full time

Job summary

Columbia University Irving Medical Center in New York seeks a highly organized Research Coordinator to oversee clinical studies at the Weinberg Family Cerebral Palsy Center. The RC will report to the Center Director of Research and the Center Manager, handling regulatory and administrative duties with precision.

Responsibilities include IRB protocol preparation, consent development, data management, subject recruitment, and collaboration with PIs.

Qualifications

• Bachelor's degree and 3 years of research experience.
• Strong organizational skills and attention to detail.
• Proficiency in English (spoken and written).

Responsibilities

• IRB protocol write-up and submission, informed consent development, HIPAA forms, data management and study file maintenance.
• On-boarding, supervision and evaluation of research staff and volunteers; supervise student projects.
• Subject screening and recruitment, data collection, chart reviews, and basic data analysis; manage study databases.

Skills

Attention to detail

English proficiency

3 years experience in research

Education

Bachelor's degree

Tools

MS Word

MS Excel

MS PowerPoint

EPIC

Adobe Acrobat

Job description

Columbia University Irving Medical Center in New York seeks a highly organized Research Coordinator to oversee clinical studies at the Weinberg Family Cerebral Palsy Center. The RC will report to the Center Director of Research and the Center Manager, handling regulatory and administrative duties with precision.

Responsibilities include IRB protocol preparation, consent development, data management, subject recruitment, and collaboration with PIs.