Clinical Research Coordinator, Part-Time

7 days ago

New York, New York, United States NYU Langone Health Full time
Job Summary

We are seeking a highly skilled and detail-oriented Research Coordinator, Part-Time to join our team at NYU Langone Health. The successful candidate will be responsible for coordinating clinical trials and research studies, ensuring the accurate execution of research protocols, and providing exceptional support to our research team.

Key Responsibilities
  • Human Subjects' Research: Oversee the submission of necessary documents required by the Institutional Review Board (IRB) and other regulatory agencies to obtain approval to conduct human subjects research.
  • Study Regulations: Ensure compliance with study regulatory status, maintain up-to-date copies of regulatory documents, and assist with the informed consent process.
  • Data Management: Collect, audit, and manage patient information for research projects, including abstraction of data from patient charts and preparation of forms and reports.
  • Budget: Develop preliminary draft budgets, review sponsor-proposed budgets, and assist with the preparation of funding reports to funding agencies.
  • Decision Making and Problem Solving: Combine and evaluate information and data to make decisions about relative importance and choose the best solution to solve problems.
  • Recruitment and Retention: Work with local recruiting partners, develop relationships with new recruiting partners, and screen potential patients/subjects for eligibility to the study.
  • Clinical Competency: Perform urine testing, handle, store, and ship specimens, and complete clinical training and didactic competency tests as required.
  • Continuous Learning: Participate in ongoing continuing education in research development, promote professional growth and development, and maintain current expertise in the area of practice.
  • Reporting and Analysis: Research, compile, and consolidate data, conduct preliminary analyzes, and provide reports to sponsoring and regulatory agencies.
  • Grants: Prepare and submit grant applications, collect and organize required paperwork, and follow up on issues and progress.
Requirements
  • Bachelor's degree or equivalent in business administration, healthcare administration, or a related field.
  • Minimum of two years of progressively responsible project coordination experience, preferably in a research setting.
  • Proficiency in using various Microsoft Office applications, including Word, Excel, Access, PowerPoint, and Outlook.
  • Effective oral, written, communication, and interpersonal skills.
  • Ability to interface effectively with all levels of management and work and communicate effectively with both internal and external customers.
  • Ability to work within a team environment as well as independently.
  • Commitment to continuous learning as required by department administration.
  • Ability to operate research-related equipment.
  • Ability to work and make decisions independently.
  • Time management skills and ability to multitask.
  • Ability to identify, analyze, and solve problems.

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