Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
IRB Coordinator
Robert Lee, TX · On-site
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
IRB Coordinator
Robert Lee, TX · On-site
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
IRB Coordinator
Addis, LA · On-site
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
IRB Coordinator
Addis, LA · On-site
Professional Hourly The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This ...
Clinical Research Coordinator - Part Time
Manhattan, NY · On-site
$48 - $52/hr
Certified Clinical Research Coordinator (CCRC) Part-Time | One Day per Week (On-Site) Location ... Strong working knowledge of GCP, ICH, FDA regulations, and IRB processes. * Experience working ...
Quick apply
Clinical Research Coordinator - Part Time
Manhattan, NY · On-site
$48 - $52/hr
Certified Clinical Research Coordinator (CCRC) Part-Time | One Day per Week (On-Site) Location ... Strong working knowledge of GCP, ICH, FDA regulations, and IRB processes. * Experience working ...
Research Program Assistant (Part-time)
Dayton, OH · On-site
$16/hr
Faculty Rank or Job Title Research Program Assistant (Part-time) Job Category: Research Department ... Familiarity with IRB processes and human subjects research. * Experience with qualitative or mixed ...
Research Program Assistant (Part-time)
Dayton, OH · On-site
$16/hr
Faculty Rank or Job Title Research Program Assistant (Part-time) Job Category: Research Department ... Familiarity with IRB processes and human subjects research. * Experience with qualitative or mixed ...
Director of Clinical Research (PT/FT)
Manhattan, NY · On-site
$150K - $228K/yr
Director of Clinical Research (PT/FT) Deliberate AI Hybrid (NYC or Boston)Full-Time or Part-Time ... You'll manage IRB submissions and regulatory compliance across our multi-site trial portfolio. And ...
Director of Clinical Research (PT/FT)
Manhattan, NY · On-site
$150K - $228K/yr
Director of Clinical Research (PT/FT) Deliberate AI Hybrid (NYC or Boston)Full-Time or Part-Time ... You'll manage IRB submissions and regulatory compliance across our multi-site trial portfolio. And ...
Adjunct PhDIT Dissertation Chair
Williamsburg, KY · On-site +1
Providing feedback and support to address IRB revisions or queries. * Provide ongoing mentorship ... Employment Type: Part-Time Location: Remote/Hybrid options available Cumberlands is different by ...
Adjunct PhDIT Dissertation Chair
Williamsburg, KY · On-site +1
Providing feedback and support to address IRB revisions or queries. * Provide ongoing mentorship ... Employment Type: Part-Time Location: Remote/Hybrid options available Cumberlands is different by ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Shift First Shift Time Type Part time Scheduled Weekly Hours 32 Cost Center 1500 Nursing ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Shift First Shift Time Type Part time Scheduled Weekly Hours 32 Cost Center 1500 Nursing ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Shift First Shift Time Type Part time Scheduled Weekly Hours 32 Cost Center 1500 Nursing ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Shift First Shift Time Type Part time Scheduled Weekly Hours 32 Cost Center 1500 Nursing ...
RESEARCH ASSOCIATE
Camden, NJ · On-site
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Completes and maintains all study documents as required by the IRB, Cooper Health System, sponsor ...
RESEARCH ASSOCIATE
Camden, NJ · On-site
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Completes and maintains all study documents as required by the IRB, Cooper Health System, sponsor ...
CLINICAL RESEARCH NURSE I
Camden, NJ · On-site
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Short Description The Clinical Research Nurse will facilitate preparation of IRB protocol ...
CLINICAL RESEARCH NURSE I
Camden, NJ · On-site
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Short Description The Clinical Research Nurse will facilitate preparation of IRB protocol ...
CLINICAL RESEARCH NURSE COORDINATOR II (PART-TIME)
Birmingham, AL · On-site
$35K - $49K/yr
... (Part-Time). General Responsibilities * To serve as primary coordinator for clinical research ... To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB ...
CLINICAL RESEARCH NURSE COORDINATOR II (PART-TIME)
Birmingham, AL · On-site
$35K - $49K/yr
... (Part-Time). General Responsibilities * To serve as primary coordinator for clinical research ... To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB ...
Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation ... Shift First Shift Time Type Part time Scheduled Weekly Hours 32 Cost Center 1500 Nursing ...
Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation ... Shift First Shift Time Type Part time Scheduled Weekly Hours 32 Cost Center 1500 Nursing ...
This is a full-time or part-time Clinical Research Coordinator position offered through Clinical ... Position-specific responsibilities • Adhere to an IRB approved protocol and submit protocol ...
This is a full-time or part-time Clinical Research Coordinator position offered through Clinical ... Position-specific responsibilities • Adhere to an IRB approved protocol and submit protocol ...
Research Assistant - Part-time
New York, NY · On-site
$30/hr
Remote or Hybrid Position PART TIME: Up to 6 hours/week through 12/31/26 Project title: Parenting ... with IRB protocols and human subjects research procedures • Experience supporting academic ...
Research Assistant - Part-time
New York, NY · On-site
$30/hr
Remote or Hybrid Position PART TIME: Up to 6 hours/week through 12/31/26 Project title: Parenting ... with IRB protocols and human subjects research procedures • Experience supporting academic ...
Clinical Affairs Manager (Part-Time)
$135 - $175/hr
About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Support hospital IRB processes and vendor vetting procedures * Lead clinical training and education ...
Clinical Affairs Manager (Part-Time)
$135 - $175/hr
About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Support hospital IRB processes and vendor vetting procedures * Lead clinical training and education ...
... IRB, and all relevant regulatory guidelines • Oversee data integrity, patient safety, and ethical conduct throughout the study • Collaborate with internal and external partners, including ...
... IRB, and all relevant regulatory guidelines • Oversee data integrity, patient safety, and ethical conduct throughout the study • Collaborate with internal and external partners, including ...
... IRB, and all relevant regulatory guidelines • Oversee data integrity, patient safety, and ethical conduct throughout the study • Collaborate with internal and external partners, including ...
... IRB, and all relevant regulatory guidelines • Oversee data integrity, patient safety, and ethical conduct throughout the study • Collaborate with internal and external partners, including ...
No Standard Hours per Week up to 19 hours Full Time or Part Time? Part Time Shift Day Work Schedule ... Reports serious AEs to IRB and sponsor. * Documents all protocol deviations, reconciles test ...
No Standard Hours per Week up to 19 hours Full Time or Part Time? Part Time Shift Day Work Schedule ... Reports serious AEs to IRB and sponsor. * Documents all protocol deviations, reconciles test ...
Part Time Irb information
See salary details
$29K - $35K
2% of jobs
$35K - $40.9K
12% of jobs
$43.8K is the 25th percentile. Wages below this are outliers.
$40.9K - $46.9K
23% of jobs
The median wage is $51.2K / yr.
$46.9K - $52.8K
18% of jobs
$52.8K - $58.8K
15% of jobs
$63.2K is the 75th percentile. Wages above this are outliers.
$58.8K - $64.7K
7% of jobs
$64.7K - $70.7K
9% of jobs
$70.7K - $76.6K
6% of jobs
$76.6K - $82.6K
3% of jobs
$82.6K - $88.5K
2% of jobs
$88.5K - $94.5K
2% of jobs
$29K
$57.3K
$94.5K
How much do part time irb jobs pay per year?
What are part-time IRB professionals?
Can you be a CRA with no experience?
What are the key skills and qualifications needed to thrive as a part-time IRB (Institutional Review Board) member, and why are they important?
What jobs pay $10,000 a month without a degree?
What jobs pay 2000 a day?
What is the difference between Part Time Irb vs Part Time Research Coordinator?
| Aspect | Part Time Irb | Part Time Research Coordinator |
|---|---|---|
| Required Credentials | Typically requires IRB certification or training, understanding of ethical guidelines | Requires research experience, often with familiarity in IRB processes, but may not need certification |
| Work Environment | Primarily administrative, reviewing research protocols for compliance | More hands-on with study management, participant interaction, and data collection |
| Employer & Industry Usage | Used by research institutions, hospitals, and universities for ethical review | Employed by research sites, hospitals, and academic institutions to coordinate studies |
While both roles are involved in research, Part Time Irb focuses on ethical review and compliance, whereas Part Time Research Coordinator handles study operations and participant management. Understanding these differences helps job seekers target the right position based on their skills and interests.
How to get an IRB job?
What are some typical responsibilities for someone in a part-time IRB (Institutional Review Board) role?
- Part Time Clinical Research Contract
- Contract Research Assistant
- No Experience Research Assistant
- Laboratory Research Assistant
- Part Time Ppd Clinical Research
- Freelance Clinical Research Assistant
- Clinical Trial Diversity
- Part Time Duke Clinical Research
- Bilingual Research Assistant
- Weekend Research Assistant

Part-time
Medical, Dental, Vision, Life, Retirement
Posted 16 days ago
Job description
The Institutional Review Board (IRB) at Louisiana State University seeks a part-time IRB Analyst to support the ethical review and oversight of human subjects research. This position is primarily on-campus in Baton Rouge.
The IRB Analyst supports protocol review processes, provides regulatory guidance to investigators, and assists in maintaining compliance with federal, state, and institutional requirements governing human subjects research.
Job Responsibilities:
Protocol Pre-Review: Conduct administrative and regulatory pre-reviews of IRB submissions, including new protocols, amendments, continuing reviews, and reportable events, to ensure completeness and compliance. (40%)
Investigator Support: Provide guidance to faculty, staff, and student researchers regarding IRB processes, submission requirements, and applicable regulations. (20%)
Meeting Coordination: Assist in preparing IRB meeting materials, including agendas and protocol assignments, and document proceedings through detailed meeting minutes. (10%)
Reliance Agreements: Support coordination of single IRB (sIRB) reliance agreements for multi-site studies, serving as a liaison between internal and external stakeholders. Data Use Agreements: Assist with processing and tracking data use agreements (DUAs) associated with IRB protocols. (10%)
Regulatory Compliance: Maintain working knowledge of applicable regulations, including the Common Rule (45 CFR 46), HIPAA, and institutional policies. (5%)
Educational Resources: Contribute to the development and maintenance of IRB guidance materials, website content, and training resources to support the research community. (5%)
Quality Assurance: Participate in internal audits and quality improvement activities to ensure ongoing compliance with regulatory and institutional standards. (5%)
Other duties as assigned. (5%)
Minimum Qualifications:
Bachelor's degree in public health, social sciences, biomedical sciences, research administration, or a related field. Basic knowledge of human subjects research protections and applicable regulations (e.g., Common Rule, HIPAA).
Candidates who have relevant experience in key job responsibilities are encouraged to apply-a degree is not required as long as the candidate meets the required years of experience specified in the job description.
Preferred Qualifications:
Bachelor's degree in public health, social sciences, biomedical sciences, research administration, or a related field. Basic knowledge of human subjects research protections and applicable regulations (e.g., Common Rule, HIPAA). Strong written and verbal communication skills. Demonstrated organizational skills and attention to detail. Ability to manage multiple priorities in a deadline-driven environment. Proficiency in Microsoft Office and electronic research administration systems. Experience in an IRB office or human subjects protection program. Familiarity with federal, state, and institutional research compliance requirements.Experience supporting IRB operations, including protocol review, meeting documentation, or multi-site research coordination.
Additional Information:
This position is in-person and part-time (20 hours per week).
Please attach ALL required documents under the "Resume/CV" section of your application.
A copy of your transcript(s) may be attached to your application (if available). However, original transcripts are required before hiring (if applicable).
Due to the nature of the position and/or position responsibilities, this position shall be subject to pre-employment screenings in accordance with University Policy as required.
For questions or concerns about updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu.
For questions or concerns regarding the status of your application or salary ranges, please contact Melissa Henderson at mesnau1@lsu.edu.Posting Date:June 4, 2026Closing Date (Open Until Filled if No Date Specified):October 2, 2026Additional Position Information:
Background Check - An offer of employment is contingent on a satisfactory pre-employment background check.
Benefits - LSU offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!
Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.
Essential Position (Y/N):LSU is an Equal Opportunity Employer.All candidates must have valid U.S. work authorization at the time of hire and maintain that valid work authorization throughout employment. Changes in laws, regulations, or government policies may impact the university's ability to employ individuals in certain positions.
HCM Contact Information:For questions or concerns related to updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu. For questions or concerns regarding the status of your application or salary ranges, please contact the department using the information provided in the Special Instructions section of this job posting.