Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional ... HRPP Support * Assist the HRPP Associate Director in daily activities * Takes the initiative in ...
Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional ... HRPP Support * Assist the HRPP Associate Director in daily activities * Takes the initiative in ...
Institutional Review Board Assistant (8a-5p) Research Institute - Kingsport, TN
Kingsport, TN · On-site
This individual will process all submissions to the IRB. This includes new applications, continuing renewals, amendments, SAEs, and other adverse event reports. The Assistant shall review claims of ...
Institutional Review Board Assistant (8a-5p) Research Institute - Kingsport, TN
Kingsport, TN · On-site
This individual will process all submissions to the IRB. This includes new applications, continuing renewals, amendments, SAEs, and other adverse event reports. The Assistant shall review claims of ...
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$59K/yr
Join Crabby Bills as a Full-Time Assistant Manager and immerse yourself in an exciting, fast-paced environment right in picturesque Indian Rocks Beach, FL. This is your opportunity to play a vital ...
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$59K/yr
Join Crabby Bills as a Full-Time Assistant Manager and immerse yourself in an exciting, fast-paced environment right in picturesque Indian Rocks Beach, FL. This is your opportunity to play a vital ...
Clinical Research Coordinator A
Philadelphia, PA · On-site
$46K/yr
... Board (IRB). * Assist in the preparation and processing of regulatory documentation with pharmaceutical companies and CROs. * Assist in obtaining the appropriate signatures for regulatory forms.
Clinical Research Coordinator A
Philadelphia, PA · On-site
$46K/yr
... Board (IRB). * Assist in the preparation and processing of regulatory documentation with pharmaceutical companies and CROs. * Assist in obtaining the appropriate signatures for regulatory forms.
$18.50 - $24.50/hr
Summary This position will assist the IRB Administrator with implementation of human subjects' protections programs at MUSC and cooperating institutions. Coordinates the IRB review process and ...
New
$18.50 - $24.50/hr
Summary This position will assist the IRB Administrator with implementation of human subjects' protections programs at MUSC and cooperating institutions. Coordinates the IRB review process and ...
New
Assistant Director, Operations
Manhattan, NY · On-site
$125 - $135/hr
Oversees OHRA review committees including IRB and ancillary commmittees within the department ... assist with the day-to-day operations of the human research protection program at Montefiore ...
Assistant Director, Operations
Manhattan, NY · On-site
$125 - $135/hr
Oversees OHRA review committees including IRB and ancillary commmittees within the department ... assist with the day-to-day operations of the human research protection program at Montefiore ...
Oversees OHRA review committees including IRB and ancillary commmittees within the department ... assist with the day-to-day operations of the human research protection program at Montefiore ...
Oversees OHRA review committees including IRB and ancillary commmittees within the department ... assist with the day-to-day operations of the human research protection program at Montefiore ...
Position Information Job Title Assistant Director, Research Compliance Union Level Department ... Fully manage IRB protocols and process and administer incoming sponsored contracts. Serves as the ...
Position Information Job Title Assistant Director, Research Compliance Union Level Department ... Fully manage IRB protocols and process and administer incoming sponsored contracts. Serves as the ...
Assistant Director, Research Compliance
Stockton, CA · On-site
$83K - $86K/yr
Posting Details Position Information Job Title Assistant Director, Research Compliance Union Level ... Fully manage IRB protocols and process and administer incoming sponsored contracts. Serves as the ...
Assistant Director, Research Compliance
Stockton, CA · On-site
$83K - $86K/yr
Posting Details Position Information Job Title Assistant Director, Research Compliance Union Level ... Fully manage IRB protocols and process and administer incoming sponsored contracts. Serves as the ...
... dementia. * Assist Pl in developing clinical trial protocols; provide clinical enrollment of ... Weinkauf's research trial; responsible for completing intake for patients and meeting IRB ...
... dementia. * Assist Pl in developing clinical trial protocols; provide clinical enrollment of ... Weinkauf's research trial; responsible for completing intake for patients and meeting IRB ...
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$59K/yr
Join Crabby Bills as a Full-Time Assistant Manager and immerse yourself in an exciting, fast-paced environment right in picturesque Indian Rocks Beach, FL. This is your opportunity to play a vital ...
Quick apply
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$59K/yr
Join Crabby Bills as a Full-Time Assistant Manager and immerse yourself in an exciting, fast-paced environment right in picturesque Indian Rocks Beach, FL. This is your opportunity to play a vital ...
IRB Operations Specialist 1 (Remote)
Cary, NC · On-site +1
$19.50/hr
WCG IRB Job Type: Full Time - Regular Description and Requirements ABOUT WCG: WCG's clinical ... Is able to assist others across Operations, as needed. This may include overtime requests, training ...
New
IRB Operations Specialist 1 (Remote)
Cary, NC · On-site +1
$19.50/hr
WCG IRB Job Type: Full Time - Regular Description and Requirements ABOUT WCG: WCG's clinical ... Is able to assist others across Operations, as needed. This may include overtime requests, training ...
New
Research Assistant I
Charleston, WV · On-site
$18.75 - $25.75/hr
... IRB and grants documentation for institutional approval, including revisions, addendums, renewals and signatures/approval as directed. • Document that IRB has been notified of a protocol change ...
Research Assistant I
Charleston, WV · On-site
$18.75 - $25.75/hr
... IRB and grants documentation for institutional approval, including revisions, addendums, renewals and signatures/approval as directed. • Document that IRB has been notified of a protocol change ...
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$52K/yr
Looking for an assistant manager who has 2+ years of experience in the hospitality field in a management position. Managers are required to work a minimum of 50 hours a week. Open availability ...
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$52K/yr
Looking for an assistant manager who has 2+ years of experience in the hospitality field in a management position. Managers are required to work a minimum of 50 hours a week. Open availability ...
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$52K/yr
Looking for an assistant manager who has 2+ years of experience in the hospitality field in a management position. Managers are required to work a minimum of 50 hours a week. Open availability ...
Quick apply
Assistant Manager - Crabby Bill's IRB
Indian Rocks Beach, FL · On-site
$52K/yr
Looking for an assistant manager who has 2+ years of experience in the hospitality field in a management position. Managers are required to work a minimum of 50 hours a week. Open availability ...
Regulatory Affairs Assistant Location: Fully onsite Join our client's clinical research team as a ... Collect and prepare regulatory documents for submission to the sponsor and IRB * Maintain current ...
New
Regulatory Affairs Assistant Location: Fully onsite Join our client's clinical research team as a ... Collect and prepare regulatory documents for submission to the sponsor and IRB * Maintain current ...
New
Clinical Research Assistant
Fairfax, VA · On-site
$46K - $96K/yr
The Clinical Research Assistant will perform a variety of duties involved in the collection ... Responsible for submissions and reports to the IRB; maintains documentation of IRB communications ...
Clinical Research Assistant
Fairfax, VA · On-site
$46K - $96K/yr
The Clinical Research Assistant will perform a variety of duties involved in the collection ... Responsible for submissions and reports to the IRB; maintains documentation of IRB communications ...
Ensure experiments comply with university and IRB policies and procedures. * Prepare reports and presentations for research team meetings. * Assist with the preparation and submission of research ...
New
Ensure experiments comply with university and IRB policies and procedures. * Prepare reports and presentations for research team meetings. * Assist with the preparation and submission of research ...
New
Knowledge of IRB and human subjects research protection regulations is desirable. Above all, the ... Complete case report forms (paper and electronic data capture) * Assist with IRB/regulatory ...
Knowledge of IRB and human subjects research protection regulations is desirable. Above all, the ... Complete case report forms (paper and electronic data capture) * Assist with IRB/regulatory ...
Clinical Research Assistant
$46K - $96K/yr
The Clinical Research Assistant will perform a variety of duties involved in the collection ... Responsible for submissions and reports to the IRB; maintains documentation of IRB communications ...
Clinical Research Assistant
$46K - $96K/yr
The Clinical Research Assistant will perform a variety of duties involved in the collection ... Responsible for submissions and reports to the IRB; maintains documentation of IRB communications ...
Irb Assistant information
What is an IRB assistant?
What skills and qualifications are needed to thrive as an IRB assistant?
What are common challenges faced by an IRB assistant and how can they be managed?
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 cities are hiring for Irb Assistant jobs?
Cities with the most Irb Assistant job openings:
What are the most commonly searched types of Irb jobs?
The most popular types of Irb jobs are:
What states have the most Irb Assistant jobs?
States with the most job openings for Irb Assistant jobs include:
What job categories do people searching Irb Assistant jobs look for?
The top searched job categories for Irb Assistant jobs are:

Part-time
Posted 25 days ago
Brigham Young University rating
7.4
Based on 88 frontline employees who took The Breakroom Quiz
338th of 620 rated colleges and universities
Job description
Why Work at BYU
As the flagship higher education institution of The Church of Jesus Christ of Latter-day Saints, Brigham Young University (BYU) strives to be among the exceptional universities in the world. At BYU, we are devoted to our faith and to our students. We take an active role in the University's Mission: "To assist individuals in their quest for perfection and eternal life."
Our unique mission, deeply rooted in the Gospel of Jesus Christ, provides countless ways to serve and make an impact. This, along with our remarkable culture of belonging, weekly devotionals, and endless opportunities for learning and growth-all situated within a beautiful and historic campus-make it an inspiring place to work.
Brigham Young University strongly prefers to hire faithful members of The Church of Jesus Christ of Latter-day Saints.
Members of The Church of Jesus Christ of Latter-day Saints must hold and be worthy to hold a current temple recommend.
HRPP Compliance Assistant - part-time/17.5 hours per week
This is a 1/2-time position that provides research campus-wide compliance support for the Human Research Protection Program (HRPP) which oversees the Institutional Review Board for Human Subjects (IRB). General responsibilities include screening human subject research studies, education outreach assistant, record keeping and other responsibilities as determined by the HRPP Associate Director; effort divided 50% to IRB and 50% to HRPP.
What you will be doing in this position
Protocol Application Coordinator
Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional regulations and policies.
Prescreens submission packets (completeness and training credentials,)
Screen for and learn to make determinations for exempt protocols
Coordinate revision of applications and amendments
Identify potential problems and issues and advise the IRB administrator.
Assist with minutes as needed, transcribe recordings, maintain record-keeping and attendance at meetings.
HRPP Support
Assist the HRPP Associate Director in daily activities
Takes the initiative in collecting technical information from a wide variety of sources.
Maintain the confidentiality of information and records with tact and discretion.
Perform other related duties and participate in special projects as assigned
Education and Training Support
Assist committee members in using OneAegis software
Assist investigators in using OneAegis software
Assist with IRB member and new member training
Assist in the creation of educational materials
Prepare and present training across campus as needed with a focus on student training
What qualifies you for this role
Minimum Education/Experience Required
- Bachelor's degree and one (1) year of experience in research administration, human subjects research, regulatory compliance, healthcare, higher education administration, or a related field; or an equivalent combination of education and experience.
- Experience interpreting and applying policies, procedures, or regulatory requirements.
- Experience managing multiple projects and deadlines in a fast-paced environment.
Preferred Qualifications
- One (1) year of experience supporting an Institutional Review Board (IRB) or Human Research Protection Program (HRPP).
- Knowledge of federal regulations and ethical principles governing human subjects research, including the Common Rule (45 CFR 46), FDA regulations, and HIPAA privacy requirements.
- Experience using electronic IRB management systems, preferably OneAegis.
- Completion of CITI Human Subjects Research or IRB Administration training.
- Experience working in a higher education, healthcare, or research environment.
Skills, Knowledge, and Abilities
- Strong written and verbal communication skills, with the ability to communicate complex regulatory requirements clearly and professionally.
- A strong attention to detail.
- Strong analytical and critical thinking skills, including the ability to interpret policies, regulations, and guidance documents.
- Excellent organizational skills with demonstrated attention to detail and the ability to manage multiple competing priorities and deadlines.
- Ability to prepare meeting materials, correspondence, determinations, and other regulatory documents with a high degree of accuracy.
- Ability to provide exceptional customer service and regulatory guidance to investigators, study teams, students, and other stakeholders.
- Strong interpersonal skills and the ability to work collaboratively and diplomatically with faculty, students, administrators, and staff.
- Proficiency with Microsoft Office Suite and database or electronic workflow systems; ability to learn and effectively use new software applications.
- Ability to exercise sound judgment, maintain confidentiality, and handle sensitive information appropriately.
- Ability to work independently while contributing effectively as a member of a team.
- Commitment to continuous learning and professional development in human research protections and research compliance.
What we offer in return
This position comes with fantasticbenefits, including:
Employeeassistanceprogram, available tothe employeeand all members of their household
Access to the library
Free on-campus parking
Free UTApass
Discounts at the BYU Store and for many events at BYU
PayGrade:48
Typical Starting Pay:$20.25-$26.50
The actual compensation offered will take into consideration internal equity and may vary based on the candidate's job-related experience, knowledge, skills, and other relevant factors. Candidates withvery significantwork-related experience may receive an offer higher than the posted typical range.
Required Documents:
All Staff positions require a resume.
Refer to the Job Posting for any additional required documents.
Brigham Young University is an equal opportunity employer, including disability and protected veteran status.
Brigham Young University (BYU) is widely recognized not just for its world-class education, but for its deep commitment to inspired religious values. Gathered together in a Christ-centered atmosphere, BYU employees are a vital part of a community of belonging, where we value the experiences, perspectives, and talents of each individual. If you share in our devotion to faith and to excellence, we have a place for you here at BYU!
What Brigham Young University employees say
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About Brigham Young University
Sourced by ZipRecruiter
Industry
Colleges, universities, and professional schools
Company size
1,001 - 5,000 Employees
Headquarters location
Provo, UT, US
Year founded
1875