Overview | 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 six centers and institutes that focus on cancer treatment and research, neuroscience, clinical and translational research, 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 including New Brunswick, Piscataway, Newark, Scotch Plains, Somerset, Blackwood, and other locations. Clinical partners include Robert Wood Johnson University Hospital in New Brunswick, University Hospital in Newark, and other affiliates.
Through this community of healers, scientists, and scholars, Rutgers is equipped as never before to transform lives. |
Posting Summary | Rutgers, The State University of New Jersey, is seeking a Clinical Research Coordinator II for the Department of Medicine, Division of Cardiovascular Diseases and Hypertension at the Rutgers Robert Wood Johnson Medical School.
This position involves the management and oversight of multiple Cardiology research studies under the guidance of the Principal Investigator. Responsibilities include overseeing study protocols, completing necessary documentation, analyzing study data, and preparing reports. This is an exceptional opportunity to contribute to groundbreaking research and have a meaningful impact on improving patient outcomes. The Research Coordinator collaborates with departmental leadership and research staff to coordinate all aspects of clinical research studies in various therapeutic areas. They independently coordinate assigned clinical research protocols from national research agencies and pharmaceutical corporations, ensuring patient screening, recruitment, protocol implementation, data collection, and submission to the Institutional Review Board (IRB).
Among the key duties of this position are the following: - Carefully collect, compile and document clinical research data according to the study protocol and sponsor guidelines.
- Maintain documentation according to protocols, standard operating procedures, and FDA requirements.
- Perform administrative tasks for the clinical research department including filing, appointment scheduling, phone follow ups, mailings, supply inventory, investigational product inventory etc
- Screen patients to identify eligible study candidates through chart review, patient interviews, discussions with practice doctors, and other methods.
- Facilitate enrollment of eligible patients by working closely with physicians and staff.
- Explain studies to eligible candidates, answer questions, and obtain written consent as delegated by the study PI and/or Research Director.
- Manage study operations on a daily basis, collaborating closely with the PI and the study team to develop and maintain project-specific timelines and status reports. Interact with the Sponsor, study sites, and internal associates, ensuring effective communication and coordination.
- Oversee study supplies and ensure proper management. Provide quality control and oversight of the internal regulatory filing system to ensure compliance with regulatory requirements.
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