Pediatric Clinical Trials Coordinator

NYU Langone Health; Village of Mineola (NY); Vor Ort; USD 59.000 - 68.000; Vollzeit

Zusammenfassung

NYU Langone Health in Mineola seeks a Research Coordinator - Clinical Trials to support regulatory and clinical activities under the Clinical Manager. The role encompasses pharmaceutical sponsored and investigator-initiated projects, from startup through recruitment and data management.

The candidate should have a Bachelor's degree, 1–2 years of related experience, and proficiency in Microsoft Office, regulatory documentation, and GCP/IRB processes. This is a full-time, on-site position.

Qualifikationen

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

Aufgaben

• Assist the clinical manager with study startup activities, pre-site visits, recruitment, enrollment and data collection.
• Ensure regulatory compliance with IRB, FDA, and study sponsors; maintain GCP/Iso compliance.
• Prepare regulatory documents and IRB submissions; manage communications with sites and sponsors.
• Support patient screening, consent processes, and follow-up visits; assist with data entry and source documentation.
• Collaborate with multidisciplinary team to conduct pediatric clinical research and educate patients and families.

Kenntnisse

CITI certification

Advanced MS Office

Ausbildung

Bachelor's Degree in related field

Tools

Microsoft Office (Excel, PowerPoint)

Jobbeschreibung

NYU Langone Health in Mineola seeks a Research Coordinator - Clinical Trials to support regulatory and clinical activities under the Clinical Manager. The role encompasses pharmaceutical sponsored and investigator-initiated projects, from startup through recruitment and data management.

The candidate should have a Bachelor's degree, 1–2 years of related experience, and proficiency in Microsoft Office, regulatory documentation, and GCP/IRB processes. This is a full-time, on-site position.