Physician Affiliate Group of New York (PAGNY) has an opportunity for a Research Coordinator at NYC Health + Hospitals/Jacobi and North Central Bronx. The Hospitals are part of NYC Health + Hospitals. Jacobi is a 457-bed, Level I Trauma Center and NCB has 213 licensed beds. The hospital maintains a strong academic affiliation with Albert Einstein Medical College to maintain its high healthcare delivery standards.   

 

The mission of NYC Health + Hospitals is to extend equally to all New Yorkers, regardless of the ability to pay, comprehensive health services of the highest quality in an atmosphere of humane care, dignity, and respect. Their Values are built on a foundation of social and racial equity and has established the ICARE standards for all staff.  

 

NYC Health + Hospitals is the nation’s largest municipal health care delivery system in the United States. Dedicated to providing the highest quality health care services to all New Yorkers with compassion, dignity and respect, and regardless of immigration status or ability to pay. 

Under general supervision, the Research Coordinator will work under the direction of the Chair of Radiology in the planning, organizing and coordination of research activities in the Radiology Department.  

 

Oversee all clinical research operations of the Radiology Department, including the administration, communication and coordination of the departments research portfolio. Facilitate and maintain required research training for personnel within the department. Work in tandem with Finance and the Associate Director of Research to prepare and submit grant applications and other grants related activity. Develop study budgets and submit to the Director/Principal Investigator for adequate coverage and recommend changes as appropriate. Prepare and oversee the submission of necessary documents required by the Institutional Board (IRB) and internal committee in order to obtain approval to conduct human subjects research. Collaborate with the Chair/PI to perform statistical analyses including preparing forms and reports, compiles and analyses data, and other materials for reports. Review scientific literature, participate in continuing education activities, and attend conferences and seminars to maintain current knowledge of clinical studies affairs As applicable, performs study coordination tasks under the direction of the investigator to ensure overall compliance in the conduct of the study, and adherence to the approved study protocol. Completes study documentation and maintains study files in accordance with sponsor requirements and institution’s policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms. Maintain effective and ongoing communication with sponsor, research participants and PI during the course of the study.