In this vital Registered Nursing role, you will coordinate ESRD patient care and services (trend lab values, track metrics on vital signs, weight, outcome management, etc.). You will ensure you and your clinical team are delivering the highest level of care to our patients by ensuring their safety, comfort, and well being.
Responsible for performing aggregate data review and trend analysis of reported safety and clinical trial data as per Clinical Data Review plan and to identify the outliers during the review and communicating the same to the Data Analyst or clinical study team as appropriate for further follow up.
The Clinical Research Coordinator manages daily operations of a biomedical and/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors and other external project stakeholders in the field of gynecologic oncology including, but not limited to, biospecimen collection studies, patient interview studies, drug intervention clinical trials, and cooperative group studies.
Coordinate and participate in a variety of clinical research studies conducted by principal investigators (physicians) including a variety of complex activities involving compilation, documentation, and analysis of clinical research data.