Pediatric Clinical Trials Coordinator

NYU Langone Health System

Village of Mineola (NY)

On-site

USD 59,000 - 68,000

Full time

5 days ago
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Benefits offered by this job

Benefits package
Wellness program

Job summary

NYU Langone Hospital-Long Island is seeking a Research Coordinator - Clinical Trials to support pediatric research across sponsored and investigator-initiated projects. You will assist the Clinical Manager with regulatory and clinical aspects of the trials.

The role involves promoting educational opportunities, ensuring compliance with GCP, IRB, and FDA, coordinating recruitment and consent processes, and managing data collection with a multidisciplinary team to advance patient care.

Qualifications

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

Responsibilities

  • Assist the clinical manager with study startup activities, recruitment, and consent processes.
  • Support regulatory documentation including IRB submissions, amendments, and communications.
  • Coordinate subject recruitment and retention, and data collection for ongoing trials.
  • Ensure compliance with GCP, ICH, FDA, and IRB regulations and guidelines.
  • Collaborate with a multidisciplinary team to conduct pediatric clinical research and education.

Skills

Communication skills
Attention to detail
Organizational skills
Team collaboration

Education

Bachelor's degree in related field
Certification in Clinical Research Coordination

Tools

Microsoft Office

Job description

NYU Langone Hospital-Long Island is seeking a Research Coordinator - Clinical Trials to support pediatric research across sponsored and investigator-initiated projects. You will assist the Clinical Manager with regulatory and clinical aspects of the trials.

The role involves promoting educational opportunities, ensuring compliance with GCP, IRB, and FDA, coordinating recruitment and consent processes, and managing data collection with a multidisciplinary team to advance patient care.

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