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 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 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 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 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 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.
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.
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.
In this role, you will perform with minimum supervision routine procedures and the most advanced procedures in at least one laboratory section or all of the routine and difficult procedures in all laboratory sections.