Heart Valve Clinical Research Coordinator

NYU Langone Health

New York (NY)

On-site

USD 66,000 - 67,000

Full time

11 days ago
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Job summary

NYU Langone Health, a leading academic medical center in New York, seeks a Research Coordinator for the Heart Valve Team to manage regulatory, operational, data, and budget aspects of complex clinical studies. The role supports investigators and study leadership and ensures compliance across multiple trials.

Ideal candidates hold a Bachelor's degree with 2+ years of research coordination experience, proficiency in MS Office, and knowledge of human subjects protections.

Qualifications

  • Minimum of two years of progressively responsible project coordination experience, preferably in a research setting.
  • Proficiency with Microsoft Word, Excel, Access, PowerPoint and Outlook; familiarity with regulatory systems.
  • Strong written and verbal communication and ability to interact with multiple stakeholders.

Responsibilities

  • Coordinate regulatory activities to obtain and maintain human subjects research approvals.
  • Oversee study operations, enrollment, compliance, and milestones across protocols.
  • Manage data handling, reporting, and study metrics for sponsors and leadership.
  • Assist with budgeting, funding projections, and financial reporting to sponsors.
  • Provide guidance to investigators and study teams on protocol requirements and regulatory expectations.
  • Support recruitment strategies and responsible participant engagement.

Skills

Project coordination
MS Office
Regulatory awareness
Communication skills

Education

Bachelor's degree or equivalent
CRC Certification (preferred)

Job description

NYU Langone Health, a leading academic medical center in New York, seeks a Research Coordinator for the Heart Valve Team to manage regulatory, operational, data, and budget aspects of complex clinical studies. The role supports investigators and study leadership and ensures compliance across multiple trials.

Ideal candidates hold a Bachelor's degree with 2+ years of research coordination experience, proficiency in MS Office, and knowledge of human subjects protections.

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