Coordinate the care of children and provide education focusing on management of diabetes and endocrine diseases; provide continuity of care for division patients and support the physicians in division goals.
Position assists investigators as research coordinator of a moderately complex clinical research study; acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.
Educates patients about drug use and disease state management, including self-monitoring, dietary considerations, warning signs, etc. Updates case report forms and source documents in a timely and accurate manner.
The Clinical Research Associate (CRA), Oncology will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Confers with PI to assist in developing plans for research projects and discuss the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate.
Position assist investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.