Research Coordinator - Inst Systems Genetics-Rsch

Job

NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care.

At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.

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We have an exciting opportunity to join our team as a Research Coordinator. This position is based in the Institute for Systems Genetics and Department of Obstetrics and Gynecology and is responsible for coordinating research studies conducted at NYU Langone Health. A core focus of this role will include enrolling pregnant individuals and coordinating associated study visits. The Research Coordinator will assist with recruitment, enrollment, grant submissions, data collection, and study coordination.

The role may also involve administrative responsibilities supporting the study Principal Investigator (PI), including scheduling, documentation, and communication. The coordinator ensures research protocols are executed in compliance with Good Clinical Practices (GCP), HIPAA, and institutional standards. They will interface directly with patients/subjects and investigators and work under general supervision.

• Participant Enrollment (OBGYN Focus):
  Screen and enroll pregnant individuals for research participation, explain the study, obtain informed consent, and coordinate study visits during pregnancy and postpartum.
• Administrative Support for PI:
  Assist the Principal Investigator with administrative tasks related to study operations, including scheduling meetings, preparing reports or presentations, tracking timelines, and communication with collaborators and regulatory bodies.
• Study Regulations:
  Maintain current regulatory documentation. Support the informed consent process and ensure participant understanding and ongoing compliance.
• Clinical
  
  Competency:
  
  May include retinal scans, specimen handling, and other tasks based on in-house training.
• Continuous Learning:
  Participate in ongoing training and demonstrate annual proof of continuing research education.
• Reporting and Analysis:
  Compile and analyze data for internal and sponsor reports. Prepare preliminary reports and assist in database management.
• Grants:
  Assist with grant applications and related activities such as proposal writing, document preparation, and progress reporting.
• Budgets:
  Help draft study budgets and prepare funding reports.
• Human Subjects' Research:
  Submit and update documentation for IRB approval and maintain compliance with institutional research oversight.
• Research
  
  Activities:
  
  Abstract data from medical records, conduct study visits, maintain logs and databases, and assist with preliminary analysis.
• Recruitment:
  Identify and screen eligible participants using medical records, physician referrals, or advertisements. Schedule and conduct initial visits and confirm eligibility with the PI.
• Special Projects:
  Participate in additional projects and duties as assigned.

To qualify you must have a Bachelor's degree in life sciences, allied health or equivalent in a related discipline and 0-1 years experience or an equivalent combination of education and experience. Effective oral, written, communication, interpersonal skills. Must be able to work under the direction of supervision. Ability to operate research related equipment. Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint and Outlook.

Familiar with Internet applications. Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure.

Knowledge of basic medical terminology is preferred. Prior experience working with Research Protocols. Experience working in an academic medical center environment.

Qualified candidates must be able to effectively communicate with all levels of the organization.

NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents. At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package.

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