Conducting Clinical Research at the Transplant Institute
We welcome interest and inquiries from researchers who wish to conduct clinical research at NYU Langone’s Transplant Institute.
Our research team comprises leading physicians in the field of research and transplantation and includes a certified clinical research coordinator and a transplant research nurse practitioner who is certified in clinical trials management and regulatory compliance.
Our team excels at providing a solid foundation for clinical trials from study startup to closure.
Study startup includes regulatory preparation, institutional review board (IRB) preparation and submissions, case report form (CRF) development, pre-study site visits, site initiation visits, laboratory billing preparation, staff education development, staff in-services, order set creation as determined by the research team, and site-specific tools to ensure study safety and efficacy.
Fees also include interim monitoring visit preparation and execution, site closure query resolution, site closure billing resolution, and site closure IRB preparation and submissions. Please note that our fees are set at a standard rate for all industry-sponsored clinical research projects and are available upon request from email@example.com.
We look forward to working with you as we pave the way to improving patient outcomes through research.