IRB Coordinator
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Robert Lee, TX ยท On-site
IRB Coordinator Position Type:Professional / Unclassified Department:LSUAM ORED - CO - Compliance Support (Douglas Lewis Villien Jr. (00011876)) Work Location:0150 Robert Lee Himes Hall Pay Grade:
Lubbock, TX ยท On-site
$15 - $33.75/hr
Review IRB applications for completeness, accuracy, clarity and congruency. You will determine action steps and document written findings for various stages of the review processes. * Ensure research ...
Lubbock, TX ยท On-site
$15 - $33.75/hr
Review IRB applications for completeness, accuracy, clarity and congruency. You will determine action steps and document written findings for various stages of the review processes. * Ensure research ...
Assists in the development of study documents and study preparation for IRB studies * Reviews and submits study protocols, informed consent forms, protocol deviations and adverse event reports, and ...
Assists in the development of study documents and study preparation for IRB studies * Reviews and submits study protocols, informed consent forms, protocol deviations and adverse event reports, and ...
Assists in the development of study documents and study preparation for IRB studies * Reviews and submits study protocols, informed consent forms, protocol deviations and adverse event reports, and ...
Assists in the development of study documents and study preparation for IRB studies * Reviews and submits study protocols, informed consent forms, protocol deviations and adverse event reports, and ...
Lubbock, TX ยท On-site
Assists with IRB meeting preparation and participates in IRB meetings, HRPP staff meetings, and professional development activities. Contributes to efforts to improve the efficiency, consistency, and ...
Lubbock, TX ยท On-site
Assists with IRB meeting preparation and participates in IRB meetings, HRPP staff meetings, and professional development activities. Contributes to efforts to improve the efficiency, consistency, and ...
Houston, TX ยท Hybrid
Prepares, facilitates, and coordinates the process for accurate and timely submission of Institutional Research Board (IRB) applications for protocol revisions or amendments to reflect any new ...
Houston, TX ยท Hybrid
Prepares, facilitates, and coordinates the process for accurate and timely submission of Institutional Research Board (IRB) applications for protocol revisions or amendments to reflect any new ...
Safeguards prior to sending to the IRB that all documents are complete and that the submission packet meets the IRB's submission requirements. * Maintains subject and document confidentiality ...
Safeguards prior to sending to the IRB that all documents are complete and that the submission packet meets the IRB's submission requirements. * Maintains subject and document confidentiality ...
Safeguards prior to sending to the IRB that all documents are complete and that the submission packet meets the IRB's submission requirements. * Maintains subject and document confidentiality ...
Safeguards prior to sending to the IRB that all documents are complete and that the submission packet meets the IRB's submission requirements. * Maintains subject and document confidentiality ...
Safeguards prior to sending to the IRB that all documents are complete and that the submission packet meets the IRB's submission requirements. * Maintains subject and document confidentiality ...
Safeguards prior to sending to the IRB that all documents are complete and that the submission packet meets the IRB's submission requirements. * Maintains subject and document confidentiality ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
This position will report directly to the Director of the NTR IRB and will also work closely with the ORC. Responsibilities include (but are not limited to) the following: 1) Assist with development ...
San Antonio, TX ยท On-site
... IRB (except to eliminate immediate hazards to the subject). o Reviews the inclusion/exclusion criteria, procedures, scheduled visits, end point criteria and investigational article use with the ...
San Antonio, TX ยท On-site
... IRB (except to eliminate immediate hazards to the subject). o Reviews the inclusion/exclusion criteria, procedures, scheduled visits, end point criteria and investigational article use with the ...
Ensure that all documents are complete, and that the submission packet meets the IRB's revision submission requirements prior to sending to the IRB * Follow-up, communicate and facilitate responses ...
Ensure that all documents are complete, and that the submission packet meets the IRB's revision submission requirements prior to sending to the IRB * Follow-up, communicate and facilitate responses ...
San Antonio, TX ยท On-site
$100K - $150K/yr
Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the proper education, training, and experience to conduct the clinical investigation. * Assume responsibility ...
Quick apply
San Antonio, TX ยท On-site
$100K - $150K/yr
Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the proper education, training, and experience to conduct the clinical investigation. * Assume responsibility ...
Perform thorough protocol pre-review in advance of submission to the Institutional Review Board (IRB) or Institutional Animal Care and Use Committee (IACUC), and provide technical consultation to ...
Perform thorough protocol pre-review in advance of submission to the Institutional Review Board (IRB) or Institutional Animal Care and Use Committee (IACUC), and provide technical consultation to ...
Perform thorough protocol pre-review in advance of submission to the Institutional Review Board (IRB) or Institutional Animal Care and Use Committee (IACUC), and provide technical consultation to ...
Perform thorough protocol pre-review in advance of submission to the Institutional Review Board (IRB) or Institutional Animal Care and Use Committee (IACUC), and provide technical consultation to ...
| Aspect | Irb | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Often requires IRB training, ethics certification | Requires research experience, sometimes certifications |
| Work Environment | Review boards, research institutions | Clinical sites, hospitals, research centers |
| Employer & Industry Usage | Used in research oversight, ethics review | Used in managing clinical trials, patient coordination |
| Common Search & Comparison Intent | Understanding roles in research ethics | Understanding clinical trial management |
IRBs (Institutional Review Boards) focus on ethical review and approval of research protocols, ensuring participant safety. Clinical Research Coordinators manage the day-to-day operations of clinical trials, including patient recruitment and data collection. While both roles are integral to clinical research, IRBs oversee ethical compliance, whereas Coordinators handle trial execution.
The most popular types of Irb jobs in Texas are:
For Irb jobs in Texas, the most frequently searched job titles are:
The top searched job categories for Irb jobs in Texas are:
Cities in Texas with the most Irb job openings:

Part-time
Medical, Dental, Vision, Life, Retirement
Re-posted 19 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.