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Cedars-Sinai Cancer is committed to pursuing pioneering research into disease mechanism, diagnostic innovations and new technologies and resources.
Through our historic achievements, growing research enterprise, and serving one of the most diverse regions in the world, our physicians and scientists are uniquely positioned to guide the next generation of progress against the disease.
Join our team and use your expertise with an organization known nationally for excellence in cancer research! The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
Evaluates and abstracts research data and ensures compliance with protocol and research objectives.
Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB.
Provides limited patient contact as needed for study and assist with study budget and patient research billing.
Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
Primary Duties and
Responsibilities:
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Provides supervised patient contact or patient contact for long term follow-up patients only.
Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
Assists with clinical trial budgets.
Assists with patient research billing.
Schedules patients for research visits and research procedures.
Responsible for sample preparation and shipping and maintenance of study supplies and kits.
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.
Participates in required training and education programs.
High School Diploma/GED Required Bachelor’s Degree in Science, Sociology or related degree (preferred) 1 year Clinical Research Related Experience (preferred) Working Title:
Clinical Research Assoc I Prdm Department:
Emergency Rm Admin Business Entity:
Service Lines & Ops Job Category:
,Academic/Research,Academic/Research Job Specialty:
Research Studies/Clinical Trials Position Type:
Per Diem Shift Length:
8 hour shift Shift Type:
Evening Recommended Skills Billing Case Report Forms Clinical Research Clinical Research Coordination Clinical Trials Data System Estimated Salary: $20 to $28 per hour based on qualifications.
Through our historic achievements, growing research enterprise, and serving one of the most diverse regions in the world, our physicians and scientists are uniquely positioned to guide the next generation of progress against the disease.
Join our team and use your expertise with an organization known nationally for excellence in cancer research! The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
Evaluates and abstracts research data and ensures compliance with protocol and research objectives.
Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB.
Provides limited patient contact as needed for study and assist with study budget and patient research billing.
Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
Primary Duties and
Responsibilities:
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Provides supervised patient contact or patient contact for long term follow-up patients only.
Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
Assists with clinical trial budgets.
Assists with patient research billing.
Schedules patients for research visits and research procedures.
Responsible for sample preparation and shipping and maintenance of study supplies and kits.
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.
Participates in required training and education programs.
High School Diploma/GED Required Bachelor’s Degree in Science, Sociology or related degree (preferred) 1 year Clinical Research Related Experience (preferred) Working Title:
Clinical Research Assoc I Prdm Department:
Emergency Rm Admin Business Entity:
Service Lines & Ops Job Category:
,Academic/Research,Academic/Research Job Specialty:
Research Studies/Clinical Trials Position Type:
Per Diem Shift Length:
8 hour shift Shift Type:
Evening Recommended Skills Billing Case Report Forms Clinical Research Clinical Research Coordination Clinical Trials Data System Estimated Salary: $20 to $28 per hour based on qualifications.
