Direct and oversee IRB operations across all campuses, ensuring compliance with federal, state, and institutional regulations; manage protocol review, approval, monitoring, and reporting processes.
Direct and oversee IRB operations across all campuses, ensuring compliance with federal, state, and institutional regulations; manage protocol review, approval, monitoring, and reporting processes.
Assistant Director, Research Compliance
Stockton, CA · On-site
$83K - $86K/yr
Direct and oversee IRB operations across all campuses, ensuring compliance with federal, state, and institutional regulations; manage protocol review, approval, monitoring, and reporting processes.
Assistant Director, Research Compliance
Stockton, CA · On-site
$83K - $86K/yr
Direct and oversee IRB operations across all campuses, ensuring compliance with federal, state, and institutional regulations; manage protocol review, approval, monitoring, and reporting processes.
Clinical Research Assistant - Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, CA · On-site
The Clinical Research Assistant independently coordinates day-to-day clinical research activities ... Prepare and submit IRB applications, amendments, continuing reviews, and reportable events ...
Clinical Research Assistant - Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, CA · On-site
The Clinical Research Assistant independently coordinates day-to-day clinical research activities ... Prepare and submit IRB applications, amendments, continuing reviews, and reportable events ...
Clinical Research Assistant - Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, CA · On-site
$39.36/hr
The Clinical Research Assistant independently coordinates day-to-day clinical research activities ... Prepare and submit IRB applications, amendments, continuing reviews, and reportable events ...
Clinical Research Assistant - Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, CA · On-site
$39.36/hr
The Clinical Research Assistant independently coordinates day-to-day clinical research activities ... Prepare and submit IRB applications, amendments, continuing reviews, and reportable events ...
Clinical Research Assistant - Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, CA · On-site
$39.36/hr
The Clinical Research Assistant independently coordinates day-to-day clinical research activities ... Prepare and submit IRB applications, amendments, continuing reviews, and reportable events ...
Quick apply
Clinical Research Assistant - Mind Body Interventions for Chronic Pain & PTSD
Palo Alto, CA · On-site
$39.36/hr
The Clinical Research Assistant independently coordinates day-to-day clinical research activities ... Prepare and submit IRB applications, amendments, continuing reviews, and reportable events ...
Senior Manager, Study Start Up
San Diego, CA · On-site
$130K - $160K/yr
Support site IRB annual reports and updates, as needed * Assist with the facilitation of the site contract and budget process * Manage translation of necessary documents through translation vendor
Senior Manager, Study Start Up
San Diego, CA · On-site
$130K - $160K/yr
Support site IRB annual reports and updates, as needed * Assist with the facilitation of the site contract and budget process * Manage translation of necessary documents through translation vendor
Clin Research Nurse - BSN - OC
Irvine, CA · On-site
... in to IRB clinical research trials. You will assist in the assessment, management and coordination of care across the continuum of care (outpatient, inpatient and home) including triage of phone ...
Clin Research Nurse - BSN - OC
Irvine, CA · On-site
... in to IRB clinical research trials. You will assist in the assessment, management and coordination of care across the continuum of care (outpatient, inpatient and home) including triage of phone ...
Clin Research Nurse - BSN - OC
Irvine, CA · On-site
... in to IRB clinical research trials. You will assist in the assessment, management and coordination of care across the continuum of care (outpatient, inpatient and home) including triage of phone ...
Clin Research Nurse - BSN - OC
Irvine, CA · On-site
... in to IRB clinical research trials. You will assist in the assessment, management and coordination of care across the continuum of care (outpatient, inpatient and home) including triage of phone ...
Clin Research Nurse - BSN - OC
Irvine, CA · On-site
... in to IRB clinical research trials. You will assist in the assessment, management and coordination of care across the continuum of care (outpatient, inpatient and home) including triage of phone ...
Clin Research Nurse - BSN - OC
Irvine, CA · On-site
... in to IRB clinical research trials. You will assist in the assessment, management and coordination of care across the continuum of care (outpatient, inpatient and home) including triage of phone ...
Junior or Assistant Specialist 2026
Irvine, CA · On-site
$26.35 - $33.87/hr
... IRB submission; 5) assisting with presentations, reports, and manuscript writing; 6) assisting with training and supervising student research assistants; and assisting with other tasks as needed.
Junior or Assistant Specialist 2026
Irvine, CA · On-site
$26.35 - $33.87/hr
... IRB submission; 5) assisting with presentations, reports, and manuscript writing; 6) assisting with training and supervising student research assistants; and assisting with other tasks as needed.
Junior or Assistant Specialist 2026
Irvine, CA · On-site
$26.35 - $33.87/hr
... IRB submission; 5) assisting with presentations, reports, and manuscript writing; 6) assisting with training and supervising student research assistants; and assisting with other tasks as needed.
Junior or Assistant Specialist 2026
Irvine, CA · On-site
$26.35 - $33.87/hr
... IRB submission; 5) assisting with presentations, reports, and manuscript writing; 6) assisting with training and supervising student research assistants; and assisting with other tasks as needed.
Clinical Research Assistant
Los Angeles, CA · On-site
The Research Assistant I provides direct support to Clinical Research Coordinators in the ... Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus. Powered ...
Quick apply
Clinical Research Assistant
Los Angeles, CA · On-site
The Research Assistant I provides direct support to Clinical Research Coordinators in the ... Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus. Powered ...
Clinical Research Assistant
Los Angeles, CA · On-site
The Research Assistant I provides direct support to Clinical Research Coordinators in the ... Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus. Powered ...
Quick apply
Clinical Research Assistant
Los Angeles, CA · On-site
The Research Assistant I provides direct support to Clinical Research Coordinators in the ... Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus. Powered ...
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
... assist primary investigators with the following tasks in order to develop ... Coordinate administrative, IRB, and/or IACUC (Institutional Animal Care and Use Committee) approval ...
Quick apply
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
... assist primary investigators with the following tasks in order to develop ... Coordinate administrative, IRB, and/or IACUC (Institutional Animal Care and Use Committee) approval ...
Clinical Research Nurse Coordinator III - Hybrid
Los Angeles, CA · On-site
$74K - $93K/yr
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Clinical Research Nurse Coordinator III - Hybrid
Los Angeles, CA · On-site
$74K - $93K/yr
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Clinical Research Nurse Coordinator III - Hybrid
Los Angeles, CA · On-site
$50.03 - $80.05/hr
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Clinical Research Nurse Coordinator III - Hybrid
Los Angeles, CA · On-site
$50.03 - $80.05/hr
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Clinical Research Nurse Coordinator III - Hybrid
Beverly Hills, CA · On-site
$79K - $99K/yr
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Clinical Research Nurse Coordinator III - Hybrid
Beverly Hills, CA · On-site
$79K - $99K/yr
Responds to all questions from the IRB or IACUC related to the regulatory aspects of the study ... May assist with grant proposals, publication preparation, and/or presentations. * May process, ship ...
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
... assist primary investigators with the following tasks in order to develop ... Coordinate administrative, IRB, and/or IACUC (Institutional Animal Care and Use Committee) approval ...
Quick apply
Clinical Research Nurse
Travis Air Force Base, CA · On-site
$47 - $60/hr
... assist primary investigators with the following tasks in order to develop ... Coordinate administrative, IRB, and/or IACUC (Institutional Animal Care and Use Committee) approval ...
Assistant Clinical Research Coordinator
Palo Alto, CA · Hybrid
$28.50 - $38/hr
Temporary Assistant Clinical Research Coordinator Responsibilities: Assist with the preparation and submission of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and ...
Quick apply
Assistant Clinical Research Coordinator
Palo Alto, CA · Hybrid
$28.50 - $38/hr
Temporary Assistant Clinical Research Coordinator Responsibilities: Assist with the preparation and submission of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and ...
Irb Assistant information
What skills and qualifications are needed to thrive as an IRB assistant?
What is the difference between Irb Assistant vs Clinical Research Coordinator?
| Aspect | Irb Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | High school diploma or associate's; some roles may require certification | Bachelor's degree often preferred; certifications like CCRP beneficial |
| Work Environment | Office and clinical settings, supporting IRB processes | Clinical sites, hospitals, or research centers managing studies |
| Employer & Industry | Research institutions, hospitals, universities | Pharmaceutical companies, research organizations, hospitals |
| Job Focus | Assisting with IRB submissions, documentation, compliance | Overseeing study coordination, patient recruitment, data collection |
The Irb Assistant primarily supports IRB-related tasks such as documentation and compliance, often requiring less extensive education. In contrast, a Clinical Research Coordinator manages the overall conduct of clinical trials, including patient interactions and data management. Both roles are essential in research but differ in scope and responsibilities.
What is an IRB assistant?
What are common challenges faced by an IRB assistant and how can they be managed?
- Clinical Research Monitor
- Microsoft Research
- Internship Clinical Psychology Research Assistant
- Research Integrity
- Law School Research Assistant
- Clinical Psychology Research Assistant
- Nextstage Clinical Research Llc
- Educational Research Assistant
- Remote Clinical Research Assistant Volunteer
- Clinical Trial Assistant

Full-time
Re-posted 11 days ago
Job description
Internal: Internal applicants will be considered within the first five (5) business days of the posting period.
External: External applicants will be considered on the sixth (6) business day of the posting period.
- Direct and oversee IRB operations across all campuses, ensuring compliance with federal, state, and institutional regulations; manage protocol review, approval, monitoring, and reporting processes. Serve as primary reviewer with authority to make not-human-subjects research and/or exemption determinations; expedited determinations; approve minor changes in not otherwise eligible for expedited review.
- Serve as a voting member and administrator of the IRB Committee, report new information, and prepare submissions for monthly convened IRB meetings.
- Manage IRB submissions and correspondence; anticipate and resolve problems; status communication of projects to leadership.
- Provide guidance, training, and regulatory interpretation to faculty, staff, and IRB members; ensure compliance with human subjects protections.
- Conduct internal and external audits of IRB and IRB protocol Principal Investigators for cause and not-for-cause; prepare annual reports and update policies in alignment with evolving regulations.
- Manage the administrative Pre-Award incoming Sponsored Contracts and verbal process, including budget review, review requirements and compliance verifications, and maintain accurate records within the Cayuse Software system.
- Review, administer and process incoming sponsored programs including contracts and grants for compliances. Support Sponsored Programs as needed.
- Manage IACUC operations, including protocol pre- review, meeting coordination, agenda/minute preparation, and regulatory reporting (OLAW/USDA).
- Prepare and submit required reports and regulatory notifications to federal agencies (e.g., OHRP, OLAW, USDA, NIH) and ensure timely compliance with applicable reporting requirements.
- Oversee animal research compliance, facility operations, inspections, and training programs in collaboration with the Attending Veterinarian and Institutional Official.
- Advises IACUC regarding potential issues affecting the use of animals in research and education. Providing administrative support to the IACUC.
- Maintain databases for protocols, animal use, training, and occupational health; ensure adherence to all applicable regulations and standards.
- Supervise and support the Animal Facility staff and coordinate post-approval monitoring activities.
- Serve as a primary liaison to campus stakeholders; provide guidance, resolve complex issues, and promote best practices in research compliance.
- Performs other duties as assigned.
- Bachelor's Degree.
- Two (2) years of experience working with IRB.
- Experience working with data.
- One (1) year of work experience in animal care and facilities.
- Experience in laboratory animal facilities management.
- Certified IRB Professional.
- Experience working with faculty and students.
- Intermediate to advanced skills in MS Office suite, and Adobe Acrobat Pro. Ability to adapt to emerging technology.
- Excellent wiring and oral communication skills.
- Excellent event/meeting scheduling and records management skills.
- Positive attitude, proven ability to work successfully with diverse populations and demonstrated commitment to promote and enhance diversity and inclusion.
- Certified Lab Animal Technician (LAT) or (ALAT) from American Association for Laboratory Animal Science (AALAS).
- Certified Professional IACUC Administrator (CPIA).
- Experience in the daily function of animal care and maintenance. Experience in a laboratory setting.
- Experience and sensitivity in working with people of diverse backgrounds and cultures.
- Demonstrated experience in advancing social justice, equity, and inclusion in a university setting.
- Ability to engage and integrate culturally responsive practices and knowledge in their work.
This is an in-person role, and the successful candidate must be willing to relocate within California, preferably within 25 miles of the Stockton Pacific campus.
Work hours may include weekends and holidays. Must respond to after-hour emergency calls when necessary.
AB 810 Misconduct Disclosure Requirement: University of the Pacific complies with California Assembly Bill 810, requiring candidates accepting conditional job offers to disclose any final administrative or judicial findings, ongoing proceedings, allegations, resignations under investigation, or appeals related to sexual harassment or misconduct within the past seven years.