Clinical Research Coordinator I Artificial Intelligence and Human Health

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profile Job Location:

New York City, NY - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Description

The Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Office).

We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to join our research team. The CRC will play a critical role in supporting two NIH-funded clinical research projects by focusing on patient recruitment participant engagement and coordination of study-related meetings. This position offers the opportunity to contribute to groundbreaking research while working closely with faculty investigators research staff and study participants



Responsibilities

Patient Recruitment & Enrollment

  • Identify screen and recruit eligible patients into study protocols.
  • Obtain informed consent in compliance with institutional and federal guidelines.
  • Serve as a primary contact for participants ensuring a positive research experience.
  • Study Coordination
    • Schedule and coordinate study-related meetings including with investigators study staff and collaborators.
    • Maintain accurate and timely study records logs and regulatory documentation.
    • Assist with scheduling participant visits follow-up calls and reminders.
  • Communication & Collaboration
    • Act as a liaison between participants investigators and the research team.
    • Coordinate with clinical and administrative staff to ensure smooth study operations.
    • Provide regular updates to the principal investigators and project managers.


Qualifications
  • Bachelors or Masters degree in Science or closely related field.
  • 1-2 years of research experience
  • Prior experience in clinical research patient recruitment or healthcare setting (preferred).
  • Strong communication organizational and interpersonal skills.
  • Ability to manage multiple priorities and work independently as well as part of a team.
  • Familiarity with IRB processes research ethics and HIPAA compliance (preferred).




Required Experience:

IC

DescriptionThe Clinical Research Coordinator assists in the daily activities of clinical research studies obtains informed consent; collects maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board Grants and Contracts Offi...
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Key Skills

  • EMR Systems
  • Employee Relations
  • Typing
  • Patient Care
  • Clerical Experience
  • HIPAA
  • Computer Skills
  • EMT Experience
  • Medical Terminology
  • Transcription
  • Epic
  • Phone Etiquette

About Company

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Strength through Unity and Inclusion The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai’s unparalleled ... View more

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