Clinical Research Coordinator II

New Jersey's academic health center, Rutgers Biomedical and Health Sciences ( RBHS) takes an integrated approach to educating students, providing clinical care, and conducting research, all with the goal of improving human health. Aligned with Rutgers University-New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and five centers and institutes that focus on cancer treatment and research, neuroscience, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research.

Our faculty are teachers, clinicians, and scientists with unparalleled experience who advance medical innovation and provide patient care informed by the latest research findings. We offer an outstanding education in medicine, dentistry, pharmacy, public health, nursing, biomedical research, and the full spectrum of allied health careers.

Our clinical and academic facilities are located throughout the state-at Rutgers University-New Brunswick, including Piscataway; and at locations in Newark, Scotch Plains, Somerset, Stratford, and other locations. Clinical partners include Robert Wood Johnson University Hospital in New Brunswick, Newark's University Hospital in Newark, and other affiliates.

Through this community of healers, scientists, and scholars, Rutgers is equipped as never before to transform lives.

Rutgers, The State University of New Jersey, is seeking a Clinical Research Coordinator II for NJMS- Medicine. The primary purpose of the Clinical Research Coordinator II ( CRCII) position is to assist a multidisciplinary and international research team with conducting clinical studies related to tuberculosis and other infectious diseases, public health, and/or clinical imaging with AI-based analyses. Role includes, but is not limited to, preparing for study initiation and activation, preparing study documents, acquisition of source documents, study monitoring visits to ensure adherence to Good Clinical Practices and study protocols, liaising and facilitating communication between team members, and data management. Provides assistance with overall study coordination that is compliant with the National Institutes of Health ( NIH), Code of Federal Regulations ( CFR), Good Clinical Practice ( CGP) guidelines, Office of Human Research Protection ( OHRP), Health Insurance Portability and Accountability Act ( HIPAA), institutional guidelines and standard operating procedures (SOPs) set forth by the department.

Among the key duties of this position are the following:

Rutgers offers a comprehensive benefit program to eligible employees. For details, please go to http://uhr.rutgers.edu/benefits/benefits-overview.

PHYSICAL DEMANDS:
Standing, sitting, walking, talking and hearing. No special vision requirements. Pushing, pulling and lifting.
WORK ENVIRONMENT: Primarily office-based setting within a research building containing laboratory and clinic facilities. Travel to international research sites (e.g. Uganda) with visits to their clinic and laboratory facilities. May work in clinical setting with possible exposure to bodily fluids and exposure to infectious and communicable diseases. Proper precautions will be taught and are mandatory.