Fresno, CA · On-site
$25 - $40.55/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Fresno, CA · On-site
$25 - $40.55/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Modesto, CA · On-site
$25 - $40.55/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Modesto, CA · On-site
$25 - $40.55/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Los Angeles, CA · On-site
$26.25 - $34.75/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Los Angeles, CA · On-site
$26.25 - $34.75/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Los Angeles, CA · On-site
$25 - $40.55/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Los Angeles, CA · On-site
$25 - $40.55/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Principal Responsibilities: Independent study ...
Los Angeles, CA · On-site
$25 - $40.55/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
Los Angeles, CA · On-site
$25 - $40.55/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
Los Angeles, CA · On-site
$25 - $40.55/hr
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 ...
Los Angeles, CA · On-site
$25 - $40.55/hr
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 ...
Beverly Hills, CA · Hybrid
$34.24 - $58.21/hr
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 ...
Beverly Hills, CA · Hybrid
$34.24 - $58.21/hr
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 ...
Los Angeles, CA · On-site
$34.24 - $58.21/hr
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 ...
Los Angeles, CA · On-site
$34.24 - $58.21/hr
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 ...
Los Angeles, CA · Hybrid
$26.25 - $34.75/hr
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 ...
Los Angeles, CA · Hybrid
$26.25 - $34.75/hr
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 ...
Los Angeles, CA · On-site
$26.25 - $34.75/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Job Duties and Responsibilities:
Los Angeles, CA · On-site
$26.25 - $34.75/hr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Job Duties and Responsibilities:
Los Angeles, CA · On-site
$72K - $123K/yr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Job Duties and Responsibilities:
Los Angeles, CA · On-site
$72K - $123K/yr
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Job Duties and Responsibilities:
Beverly Hills, CA · Hybrid
$25 - $40.55/hr
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 ...
Beverly Hills, CA · Hybrid
$25 - $40.55/hr
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 ...
Pittsburgh, PA · On-site
$23.50 - $31.25/hr
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data ...
Pittsburgh, PA · On-site
$23.50 - $31.25/hr
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Assists with training staff. Ensures adherence to protocols and corrects issues with data ...
$25 - $40.55/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
$25 - $40.55/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
Los Angeles, CA · On-site
$26.25 - $34.75/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
Los Angeles, CA · On-site
$26.25 - $34.75/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
Pittsburgh, PA · On-site
$23.50 - $31.25/hr
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Recruits research subjects and conducts interviews and research assessments.
Pittsburgh, PA · On-site
$23.50 - $31.25/hr
Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Recruits research subjects and conducts interviews and research assessments.
Los Angeles, CA · On-site
$25 - $40.55/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
Los Angeles, CA · On-site
$25 - $40.55/hr
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation. * Ensures compliance with all federal and local ...
$51K - $58.5K
13% of jobs
$58.5K - $66K
7% of jobs
$67.6K is the 25th percentile. Wages below this are outliers.
$66K - $73.5K
23% of jobs
The median wage is $76.4K / yr.
$73.5K - $81K
18% of jobs
$81K - $88.5K
11% of jobs
$94.6K is the 75th percentile. Wages above this are outliers.
$88.5K - $96K
4% of jobs
$96K - $103.5K
12% of jobs
$103.5K - $111K
7% of jobs
$111K - $118.5K
3% of jobs
$118.5K - $126K
1% of jobs
$126K - $133.5K
1% of jobs
$51K
$83.7K
$133.5K
Professionals working on an Institutional Review Board often navigate the complex balance between facilitating innovative research and upholding strict ethical standards to protect human subjects. One common challenge is keeping current with frequently evolving regulations and interpreting how they apply to a wide range of research proposals. IRB members must also manage high volumes of submissions and coordinate with researchers, legal advisors, and compliance officers to resolve issues promptly. This role requires continuous professional development and a collaborative approach to problem-solving in a multidisciplinary setting.
To thrive as an Institutional Review Board (IRB) member or administrator, you need a strong understanding of research ethics, federal regulations, and compliance requirements, often supported by a background in health sciences, law, or ethics. Familiarity with electronic IRB management systems, regulatory databases, and training in human subjects research protection (such as CITI certification) is typically required. Attention to detail, critical thinking, and the ability to communicate diplomatically with diverse stakeholders are crucial soft skills. These abilities are essential to ensure the ethical review and approval of research projects, safeguarding participants and maintaining institutional integrity.
An IRB professional is responsible for reviewing research studies involving human subjects to ensure they meet ethical and regulatory standards. They assess protocols for compliance with federal, state, and institutional guidelines to protect participant rights and welfare. Their duties include reviewing applications, providing guidance to researchers, and ensuring informed consent processes are properly implemented. IRB professionals often work in universities, hospitals, or research institutions.
$25 - $40.55/hr
Full-time
Re-posted 19 days ago
8.6
Based on 131 frontline employees who took The Breakroom Quiz
40th of 1,055 rated hospitals
Come join the Kidney Transplant Team!
The Clinical Research Coordinator I works independently providing study coordination, 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 study information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Principal Responsibilities:
Independent 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.
Schedules 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 visits, aid in site initiation visits (SIVs), perform close-out visits (COVs), and auditing activities.
Communicate with sponsors regarding exceptions and protocol clarifications.
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 perform 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.
Participates in required training and education programs
QualificationsEducation:
High School Diploma/GED, required
Bachelor's Degree, Science, Sociology or related degree, preferred
Work Experience:
1 year Clinical research related experience required
Licenses and Certifications:
Certification In Clinical Research SOCRA or ACRP certification Upon Hire preferred
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Hospitals, outpatient health care and health care and social assistance
10,000+ Employees
Los Angeles, CA, US
