Pediatric Clinical Trials Research Coordinator

NYU Langone; Village of Mineola (NY); On-site; USD 59,000 - 68,000; Full time

Job summary

NYU Langone Hospital—Long Island is seeking a Research Coordinator - Clinical Trials (Mineola) to support the Clinical Manager with pediatric research activities across pharmaceutical sponsored and investigator-initiated projects.

The role involves regulatory documentation, recruitment and data management, ensuring compliance with GCP/IRB and FDA requirements. A Bachelor's degree and 1–2 years of related experience are required, with CITI training within one month of employment.

Qualifications

• Bachelor's Degree in a related field required.
• CITI training or within 1 month of employment required.
• 1–2 years of experience in pediatrics or perinatal or related area; advanced knowledge of Microsoft Office (Excel and PowerPoint). Database management and informatics.

Responsibilities

• Supports the clinical manager with promotion of educational opportunities to increase public awareness of the pediatric clinical research program.
• Ensures compliance with hospital, departmental, safety policies and regulatory requirements (Joint Commission, IRB, FDA, study sponsors).
• Maintains certifications such as CITI and Good Clinical Practice (GCP).
• Assists with study start-up activities, pre-site visits, subject recruitment and retention, informed consent process and data collection/entry.
• Handles regulatory documentation including IRB communications, submissions, protocol/consent approvals, amendments, and adverse events.
• Coordinates patient screening, recruitment, consent, enrollment, follow-up visits and data collection (CRF/EDC) under supervision.

Skills

Database management

Research coordination

Education

Bachelor's Degree in a related field

Tools

Microsoft Office (Excel and PowerPoint)

Job description

NYU Langone Hospital—Long Island is seeking a Research Coordinator - Clinical Trials (Mineola) to support the Clinical Manager with pediatric research activities across pharmaceutical sponsored and investigator-initiated projects.

The role involves regulatory documentation, recruitment and data management, ensuring compliance with GCP/IRB and FDA requirements. A Bachelor's degree and 1–2 years of related experience are required, with CITI training within one month of employment.