Clinical Research Coordinator for HCM Trials

NYU Langone Hospitals; New York (NY); On-site; USD 66,000 - 67,000; Full time

Job summary

NYU Langone Health's NYU Grossman School of Medicine invites applications for a Research Coordinator on the Hypertrophic Cardiomyopathy Team. The role coordinates moderate to advanced study activities, supports recruitment, enrollment, grant submissions, and data collection in accordance with Good Clinical Practices, HIPAA, and sponsor requirements.

You will liaise with Research Nurses, Pharmacists, Program Managers, and IT/regulatory staff, monitor study progress, assist with budget

Qualifications

• Bachelor degree in business administration, health care administration or related field.
• Minimum of two years of progressively responsible project coordination experience, preferably in a research setting.
• Proficiency in using Microsoft Office applications such as Word, Excel, Access, Power Point and Outlook.
• Effective oral, written, communication, interpersonal skills.

Responsibilities

• Prepares and submits grant applications and other related grants/proposals.
• Oversees IRB submissions and regulatory documents for human subjects research.
• Maintains study regulatory documents and informed consent process.
• Collects, audits, and analyzes data; prepares reports.
• Develops preliminary study budgets and supports funding reports.
• Assists in recruitment and screening of study participants.
• Monitors safety and reports to PI and study team.
• Coordinates with research nurses, pharmacists, and regulatory staff.
• Supports continuing education and professional development.

Skills

Communication skills

Interpersonal skills

Education

Bachelor degree in business administration, health care administration or related field

Tools

Microsoft Office

Job description

NYU Langone Health's NYU Grossman School of Medicine invites applications for a Research Coordinator on the Hypertrophic Cardiomyopathy Team. The role coordinates moderate to advanced study activities, supports recruitment, enrollment, grant submissions, and data collection in accordance with Good Clinical Practices, HIPAA, and sponsor requirements.

You will liaise with Research Nurses, Pharmacists, Program Managers, and IT/regulatory staff, monitor study progress, assist with budget