The Clinical Practice Coordinator (CPC) is an integral part of the Dignity Health Medical Foundation (DHMF) care team. The CPC performs the functions of assessing, planning, implementing and evaluating plans of care for attributed patients.
The Clinical Lab Scientist II serves as a lead technologist in the daily production of the HLA section, performing and interpreting test results. Provides technical support to staff. Knowledge of HLA methods and molecular testing preferred. Performs specific lead functions: Reviews and implements quality control and quality assurance activities, provides staff training.
The Clinical Research Coordinator III in addition to the duties and responsibilities of a CRC II, the CRC III has added responsibilities which include assisting with the training of new staff, providing assistance with TACL protocol development, developing policies and procedures, and supporting regulatory submissions (e.g. IND applications and maintenance, MedWatch forms, IRB application and renewal, etc.).
The Clinical Laboratory Scientist is responsible for performing moderately complex and complex laboratory tests, as defined by CLIA, in hematology, chemistry, urinalysis, microbiology, blood bank and serology.
The Clinical Research Nurse (CRN) is a registered nurse who shares responsibility with the principal investigators to ensure that clinical investigations are conducted in accordance with the requirements of all regulatory agencies.
The Clinical Laboratory Scientist II ( CLS II ) functions with minimal direction from supervisory personnel. Responsibilities include blood and platelet collections, quality assurance audits in blood donor collections.
The Clinical Research Coordinator II serves as clinical research project manager on several additional externally-funded research projects in Hematology Oncology. Contributes to design of research projects to meet proposal goals established by the PI and sponsor.
The Clinical Research Coordinator II is primarily responsible for clinical data mining and database input. The CRC serves as the primary source for faculty and staff for clinical data and program outcomes and performs data queries and analyses.
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.
As a Molecular Clinical Laboratory Scientist, you will be responsible for performing high complexity testing, analyzing, reviewing, and reporting test results and quality control results, as well as taking remedial action when indicated.
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
In this role, the selected candidate will establish ongoing communication with patients during and between scheduled appointments to promote care coordination and timely delivery of services and treatments.
The Clinical Research Nurse is a Registered Nurse (RN) who works collaboratively with physicians, Clinical Research Associates (CRA) and pharmacists to coordinate care for an assigned population of patients who are enrolled in to IRB clinical research trials.