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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
HRPP Compliance Assistant - part-time/17.5 hours per week This is a 1/2-time position that provides ... Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional ...
HRPP Compliance Assistant - part-time/17.5 hours per week This is a 1/2-time position that provides ... Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional ...
Clinical Research Associate - Part Time MFM Clinical Study Grant The Clinical Research Associate ... Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
Clinical Research Associate - Part Time MFM Clinical Study Grant The Clinical Research Associate ... Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
Clinical Research Associate - Part Time MFM Clinical Study Grant The Clinical Research Associate ... Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
Clinical Research Associate - Part Time MFM Clinical Study Grant The Clinical Research Associate ... Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
HRPP Compliance Assistant - part-time/17.5 hours per week This is a 1/2-time position that provides ... Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional ...
HRPP Compliance Assistant - part-time/17.5 hours per week This is a 1/2-time position that provides ... Supports the day-to-day functions of the IRB in accordance with federal, state, and institutional ...
... Board (IRB) modifications with supporting documentation. * Maintain oversight of designated research project study activities including performing the following functions: Subject recruitment ...
... Board (IRB) modifications with supporting documentation. * Maintain oversight of designated research project study activities including performing the following functions: Subject recruitment ...
Grand Blanc, MI · Hybrid
... IRB members and research staff: * Develops and presents monthly education sessions. * Coordinates ... Schedule: Part-time * Requisition ID: 26001619 * Daily Work Times: Standard Business Hours * Hours ...
Grand Blanc, MI · Hybrid
... IRB members and research staff: * Develops and presents monthly education sessions. * Coordinates ... Schedule: Part-time * Requisition ID: 26001619 * Daily Work Times: Standard Business Hours * Hours ...
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 ...
This will be a part-time position at about 8 hours per week, never to exceed over 19.99 hours per ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
This will be a part-time position at about 8 hours per week, never to exceed over 19.99 hours per ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
Camden, NJ · On-site
$56/hr
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Facilitates preparation of IRB protocol submissions and informed consent forms. * Key individual in ...
Camden, NJ · On-site
$56/hr
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Facilitates preparation of IRB protocol submissions and informed consent forms. * Key individual in ...
Durham, NC · On-site
$60 - $85/hr
Provide training for investigators, IRB members, and staff of the OHRC in federal regulations, NIH policies and guidance related to both Title 21 and Title 45 of the Codeof Federal Regulations
Durham, NC · On-site
$60 - $85/hr
Provide training for investigators, IRB members, and staff of the OHRC in federal regulations, NIH policies and guidance related to both Title 21 and Title 45 of the Codeof Federal Regulations
This will be a part-time position at about 8 hours per week, never to exceed over 19.99 hours per ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
This will be a part-time position at about 8 hours per week, never to exceed over 19.99 hours per ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
This will be a part-time position at about 8 hours per week, never to exceed over 19.99 hours per ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
This will be a part-time position at about 8 hours per week, never to exceed over 19.99 hours per ... May prepare IRB documents under the direction of the Principal Investigator and assists with ...
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 ...
Camden, NJ · On-site
$56/hr
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Facilitates preparation of IRB protocol submissions and informed consent forms. * Key individual in ...
Camden, NJ · On-site
$56/hr
Cooper offers full and part-time employees a comprehensive benefits program, including health ... Facilitates preparation of IRB protocol submissions and informed consent forms. * Key individual in ...
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 ...
$29K - $35K
2% of jobs
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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
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9% of jobs
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$29K
$57.3K
$94.5K
| 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.
Cities with the most Part Time Irb job openings:
The most popular types of Irb jobs are:
States with the most job openings for Part Time Irb jobs include:
The top searched job categories for Part Time Irb jobs are:

Part-time
Medical, Dental, Vision, Life, Retirement
Re-posted 17 days ago
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).
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.