IRB Analyst II
Align yourself with an organization that has a reputation for excellence! Cedars-Sinai was awarded the National Research Corporation's Consumer Choice Award 19 years in a row for providing the highest-quality medical care in Los Angeles.
We were also awarded the Advisory Board Company's Workplace of the Year.
This recognizes hospitals and health systems nationwide that have outstanding levels of employee engagement.
Join us! Discover why U.
S.
News & World Report has named us one of America's Best Hospitals.
The IRB Analyst II processes moderate to high complex protocols reviews and processes submissions for IRB review.
The IRB Analyst II assumes a lead role in Departmental outreach, training, education, and quality improvement activities under the direction of the Associate Director.
Primary Duties and ResponsibilitiesoMaintains responsibility for protocols submitted for IRB review, demonstrating leadership, expertise, and assumes responsibility for the processing of protocols of moderate to high complexity that typically require the development of unique solutions or advanced understanding of the principles and regulations related to human subject researchoPerforms pre-committee analysis of protocols confirming completeness and compliance with regulations and IRB policies; determines the most expeditious processing mechanism allowed for an application and recommending this method to IRB reviewers; attends IRB meetings and provides technical support and guidance on regulatory matters; writes comprehensive meeting minutes outlining the ethical and medical issues analyzed by the committee; and accurately documents the final determinations of the IRB.
oComposes clear, concise and detailed correspondence to investigators to ensure that the concerns, rationale, and technical questions of the IRB are quickly and intelligibly communicated to the researchers; conducting staff evaluation of investigator's response to identify potential issues for IRB reviewers; issuing approval documents; and maintaining accurate updates in the Departmental online submission and tracking system.
oParticipates in educational activities for investigators, IRB members, and IRB Analyst new staff, completing projects as assigned by the Associate Director.
As requested, the IRB Analyst II provides technical support and regulatory guidance to investigators, IRB members, and new staff.
oSupports and contributes to the publication of the IRB Exchange, the newsletter for the human subject research community.
oMay participate in departmental quality improvement activities by identifying needs in department operations and making recommendations for their improvement, focusing on continued improvement of the Departmental online submission and tracking application, workflow and activities related to IRB processing; supporting the quarterly IRB 101 educational program; and assisting with other special projects as assigned.
oSupports the IRB Live Chat program as primary point of contact with the research community and resources related to the preparation and submission of applications for IRB review.
Educational Requirements:
BA /BS degree minimum
Experience:
2-3 years experience of Direct IRB or regulatory affairs experience Physical Demands:
Walking, sitting, standing.
Primary duties require computer work.
Recommended Skills Ethics Human Subject Research Leadership Networking Quality Management Technical Support Estimated Salary: $20 to $28 per hour based on qualifications.
We were also awarded the Advisory Board Company's Workplace of the Year.
This recognizes hospitals and health systems nationwide that have outstanding levels of employee engagement.
Join us! Discover why U.
S.
News & World Report has named us one of America's Best Hospitals.
The IRB Analyst II processes moderate to high complex protocols reviews and processes submissions for IRB review.
The IRB Analyst II assumes a lead role in Departmental outreach, training, education, and quality improvement activities under the direction of the Associate Director.
Primary Duties and ResponsibilitiesoMaintains responsibility for protocols submitted for IRB review, demonstrating leadership, expertise, and assumes responsibility for the processing of protocols of moderate to high complexity that typically require the development of unique solutions or advanced understanding of the principles and regulations related to human subject researchoPerforms pre-committee analysis of protocols confirming completeness and compliance with regulations and IRB policies; determines the most expeditious processing mechanism allowed for an application and recommending this method to IRB reviewers; attends IRB meetings and provides technical support and guidance on regulatory matters; writes comprehensive meeting minutes outlining the ethical and medical issues analyzed by the committee; and accurately documents the final determinations of the IRB.
oComposes clear, concise and detailed correspondence to investigators to ensure that the concerns, rationale, and technical questions of the IRB are quickly and intelligibly communicated to the researchers; conducting staff evaluation of investigator's response to identify potential issues for IRB reviewers; issuing approval documents; and maintaining accurate updates in the Departmental online submission and tracking system.
oParticipates in educational activities for investigators, IRB members, and IRB Analyst new staff, completing projects as assigned by the Associate Director.
As requested, the IRB Analyst II provides technical support and regulatory guidance to investigators, IRB members, and new staff.
oSupports and contributes to the publication of the IRB Exchange, the newsletter for the human subject research community.
oMay participate in departmental quality improvement activities by identifying needs in department operations and making recommendations for their improvement, focusing on continued improvement of the Departmental online submission and tracking application, workflow and activities related to IRB processing; supporting the quarterly IRB 101 educational program; and assisting with other special projects as assigned.
oSupports the IRB Live Chat program as primary point of contact with the research community and resources related to the preparation and submission of applications for IRB review.
Educational Requirements:
BA /BS degree minimum
Experience:
2-3 years experience of Direct IRB or regulatory affairs experience Physical Demands:
Walking, sitting, standing.
Primary duties require computer work.
Recommended Skills Ethics Human Subject Research Leadership Networking Quality Management Technical Support Estimated Salary: $20 to $28 per hour based on qualifications.
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