Clinical Research Coordinator III Spine

Company: Cedars-Sinai
Location: Alhambra
Posted on: May 24, 2023

Job Description:

The Clinical Research Coordinator III 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 oversight of all studies with the group and the assignment of studies to clinical research personnelwithin the group, and supervision of research staff. Plans and coordinates strategies for increasing patient enrollment, improving efficiency, training of personnel, and 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 Responsibilities--- Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medicaltrial 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) thefollowing; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response tostudy drug.--- Maintains accurate source documents related to all research procedures.--- Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response tosponsor 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 researchbilling and reconciliation.--- Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and localInstitutional Review Board.--- Maintains research practices using Good Clinical Practice (GCP) guidelines.--- Maintains strict patient confidentiality according to HIPAA regulations and applicable law.--- Participates in required training and education programs.--- Works with Training and Education Coordinator to ensure all staff is properly trained and certified.--- Participate in centralized activities such as auditing, Standard Operating Procedure development, etc.--- Plans and coordinates strategies for increasing patient enrollment, and/or improving clinical research efficiency.--- Identify quality and performance improvement opportunities and collaborate with staff in the development of action plansto improve quality.--- Identifies new research opportunities and presents to investigators.--- Supervises other research staff.High School Diploma/GED4-years clinical research related experience Working Title: Clinical Research Coordinator III SpineDepartment: Dept of OrthopaedicsBusiness Entity: Cedars-Sinai Medical CenterJob Category: Academic/ResearchJob Specialty: Research Studies/Clinical TrialsPosition Type: Full-timeShift Length: 8 hour shiftShift Type: DayBase Pay:$71,300.00 - $121,000.00

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