In this role, you will be responsible for improving the overall quality and completeness of clinical documentation. Promotes a partnership between the concurrent clinical reviewers, medical record coders, and physicians to improve documentation and reimbursement for PRMC.
Responsible to the Laboratory Leadership for ensuring his/her area of responsibility meets licensure/inspection requirements at all times, that all quality control is performed, documented according to policy and procedure, and that staff is properly trained.
In this role, you will be responsible to recruit, educate, and obtain study subject enrollment and consent. Complete case report forms, maintain up-to-date research logs, schedule appointments, prepare recruitment patient letters, and various other study correspondence as required.
Assure that the documentation for the clinical trial is completed and accurate. The clinical research nurse actively participates in planning and evaluation processes to improve and advance clinical research within the organization. The clinical research nurse in oncology fulfills the role in congruence with oncology nursing society competency guidelines for clinical research nurses.
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.
In this role, you will be responsible for a variety of high-complexity, clinical laboratory testing in Chemistry, Hematology, Microbiology & Blood Bank; perform QC/QA procedures, preventive maintenance & test validation.
In this role, the selected candidate will be responsible to provides input into the development of clinical monitoring plan, informed consent forms, template source documents, study manual, regulatory binder and other study-related documents as needed.
In this role, you will be responsible to perform site monitoring visits in accordance with the study monitoring plan to ensure compliance with the investigational plan, monitoring plan, applicable regulator.
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.