Cardiology Research Coordinator - Flexible Hours

NYU Langone Health; New York (NY); Presencial; USD 66.000 - 67.000; Tempo integral

Benefícios oferecidos por esta vaga

Benefits and wellness package

Resumo da vaga

NYU Langone Health is hiring a Research Coordinator to manage regulatory oversight for human-subjects studies within the Cardiology divisions. The role includes coordinating IRB submissions, ensuring protocol adherence, and liaising with investigators and sponsors.

The position supports recruitment, data collection, and study operations, with responsibilities spanning protocol compliance, patient coordination, and performance reporting in a university medical center setting.

Qualificações

• Bachelor degree or equivalent 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 various Microsoft Office applications such as Word, Excel, Access, PowerPoint and Outlook.
• Effective oral, written, communication, interpersonal skills.
• Ability to interface effectively with all levels of management and internal/external customers.
• Ability to operate research related equipment and work independently.

Responsabilidades

• Independently coordinates and oversees the regulatory lifecycle for assigned human-subjects research studies.
• Interprets study and institutional requirements; identifies documentation gaps and submission priorities; develops recommendations in consultation with PI and study team.
• Leads or facilitates the informed-consent process and coordinates participant follow-up and scheduling.
• Prepares and delivers accurate reports on study progress, enrollment, and regulatory status.

Conhecimentos

Regulatory coordination

Data management

Clinical research

Project coordination

Communication

Formação

Bachelor degree or equivalent in health care administration

Descrição da vaga

NYU Langone Health is hiring a Research Coordinator to manage regulatory oversight for human-subjects studies within the Cardiology divisions. The role includes coordinating IRB submissions, ensuring protocol adherence, and liaising with investigators and sponsors.

The position supports recruitment, data collection, and study operations, with responsibilities spanning protocol compliance, patient coordination, and performance reporting in a university medical center setting.