Kidney Transplant Clinical Research Coord II
Company: CEDARS-SINAI
Location: Fresno
Posted on: November 20, 2024
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Job Description:
Job DescriptionThe Clinical Research Coordinator II works
independently providing study coordination including screening of
potential patients for protocol eligibility, presenting non-medical
trial concepts and details, and participating in the informed
consent process. Responsible for accurate and timely source
documents, data collection, documentation, entry, and reporting
including timely response to sponsor queries. Responsible for
compiling and reporting on each study including information related
to protocol activity, accrual data, workload, and other research
information. Presents information at regular research staff
meetings. May plan and coordinate strategies for increasing patient
enrollment, improving efficiency, training of personnel, or
identifying new research opportunities. Ensures compliance with all
federal and local agencies including the Food and Drug
Administration (FDA) and local Institutional Review Board
(IRB).Primary Duties and ResponsibilitiesIndependent study
coordination including screening of potential patients for protocol
eligibility, presenting non-medical trial concepts and details to
the patients, and participating in the informed consent
process.Scheduling of patients for research visits and
procedures.In collaboration with the physician and other medical
personnel, documents thoroughly on Case Report Forms (CRFs) the
following; changes in patient condition, adverse events,
concomitant medication use, protocol compliance, response to study
drug.Maintains accurate source documents related to all research
procedures.Responsible for accurate and timely data collection,
documentation, entry, and reporting including timely response to
sponsor queries.Schedules and participates in monitoring and
auditing activities.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.Notifies direct
supervisor about concerns regarding data quality and study
conduct.Works closely with a regulatory coordinator or directly
with the Institutional Review Board (IRB) to submit Adverse Events,
Serious Adverse Events, protocol deviations, and Safety Letters in
accordance with local and federal guidelines.May involve other
regulatory / Institutional Review Board duties, budgeting duties,
and assisting with patient research billing and
reconciliation.Ensures compliance with all federal and local
agencies including the Food and Drug Administration (FDA and local
Institutional Review Board.Maintains research practices using Good
Clinical Practice (GCP) guidelines.Maintains strict patient
confidentiality according to HIPAA regulations and applicable
law.May coordinate training and education of other personnel.May
participate in centralized activities such as auditing, Standard
Operating Procedure development, etc.May plan and coordinate
strategies for increasing patient enrollment, and/or improving
clinical research efficiency.May identify quality and performance
improvement opportunities and collaborate with staff in the
development of action plans to improve quality.May identify new
research opportunities and present to investigators
QualificationsQualifications:
Req ID : 1435
Working Title : Kidney Transplant Clinical Research Coord II
Department : Research - Hepatology
Business Entity : Cedars-Sinai Medical Center
Job Category : Academic / Research
Job Specialty : Research Studies/ Clin Trial
Overtime Status : EXEMPT
Primary Shift : Day
Shift Duration : 8 hour
Base Pay : $58,864 - $100,068
Keywords: CEDARS-SINAI, Porterville , Kidney Transplant Clinical Research Coord II, Healthcare , Fresno, California
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