Project Associate Manager
Ann Arbor, MI · On-site
Job Summary The Project Manager provides comprehensive operational leadership for a ... Experience with human subjects research regulations and IRB submissions. Knowledge of MTAs, DUAs ...
Project Associate Manager
Ann Arbor, MI · On-site
Job Summary The Project Manager provides comprehensive operational leadership for a ... Experience with human subjects research regulations and IRB submissions. Knowledge of MTAs, DUAs ...
Knowledge of research compliance regulations (IRB, IACUC, IBC), grant management, and laboratory safety practices is highly desirable * Experience with process documentation, workflow mapping, and/or ...
Knowledge of research compliance regulations (IRB, IACUC, IBC), grant management, and laboratory safety practices is highly desirable * Experience with process documentation, workflow mapping, and/or ...
Clinical Research Coordinator Senior/Intermediate
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
Lead study start-up and ongoing regulatory management: IRB submissions and amendments, MTAs, DUAs, and related regulatory documents; serve as primary study team liaison across participating sites
Clinical Research Coordinator Senior/Intermediate
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
Lead study start-up and ongoing regulatory management: IRB submissions and amendments, MTAs, DUAs, and related regulatory documents; serve as primary study team liaison across participating sites
Research Assistant - Department of Oncology
Detroit, MI · On-site
$19 - $26.25/hr
Managing or supporting IRB and regulatory compliance; Literature reviews, including searching, organizing, and synthesizing research evidence; Qualitative and/or quantitative data analysis;
Research Assistant - Department of Oncology
Detroit, MI · On-site
$19 - $26.25/hr
Managing or supporting IRB and regulatory compliance; Literature reviews, including searching, organizing, and synthesizing research evidence; Qualitative and/or quantitative data analysis;
ASST IN RESEARCH (TEMP)
Ann Arbor, MI · On-site
$20/hr
Experience supporting human subjects research or Institutional Review Board (IRB) submissions. * Experience with data entry and database management (e.g., REDCap, Qualtrics, or similar systems)
ASST IN RESEARCH (TEMP)
Ann Arbor, MI · On-site
$20/hr
Experience supporting human subjects research or Institutional Review Board (IRB) submissions. * Experience with data entry and database management (e.g., REDCap, Qualtrics, or similar systems)
Knowledge of research compliance regulations (IRB, IACUC, IBC), grant management, and laboratory safety practices is highly desirable * Experience with process documentation, workflow mapping, and/or ...
Knowledge of research compliance regulations (IRB, IACUC, IBC), grant management, and laboratory safety practices is highly desirable * Experience with process documentation, workflow mapping, and/or ...
Physician Assistant (Associate) - Clinical Research
Southfield, MI · On-site
$91K - $124K/yr
... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ... Manages scheduled visits, review queues, signatures, queries, and follow-up within required ...
Physician Assistant (Associate) - Clinical Research
Southfield, MI · On-site
$91K - $124K/yr
... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ... Manages scheduled visits, review queues, signatures, queries, and follow-up within required ...
... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ... Manages scheduled visits, review queues, signatures, queries, and follow-up within required ...
... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ... Manages scheduled visits, review queues, signatures, queries, and follow-up within required ...
Physician Assistant (Associate) - Clinical Research
Southfield, MI · On-site
$91K - $123K/yr
... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ... Manages scheduled visits, review queues, signatures, queries, and follow-up within required ...
Quick apply
Physician Assistant (Associate) - Clinical Research
Southfield, MI · On-site
$91K - $123K/yr
... the IRB-approved plan, sponsor requirements, and organizational procedures. This role does not ... Manages scheduled visits, review queues, signatures, queries, and follow-up within required ...
Coordinate, manage quality control for, and liaise with vendors for high-throughput proteomic assay ... Support study operations under Good Clinical Practice (GCP) and IRB compliance requirements
Coordinate, manage quality control for, and liaise with vendors for high-throughput proteomic assay ... Support study operations under Good Clinical Practice (GCP) and IRB compliance requirements
Research Coordinator
Grand Rapids, MI · On-site
This role oversees research-related data collection and management activities, maintains accurate documentation, supports compliance and IRB processes, and assists with data analysis and reporting.
Research Coordinator
Grand Rapids, MI · On-site
This role oversees research-related data collection and management activities, maintains accurate documentation, supports compliance and IRB processes, and assists with data analysis and reporting.
This role oversees research-related data collection and management activities, maintains accurate documentation, supports compliance and IRB processes, and assists with data analysis and reporting.
This role oversees research-related data collection and management activities, maintains accurate documentation, supports compliance and IRB processes, and assists with data analysis and reporting.
Knowledge of scientific integrity principles, responsible conduct of research, and human subject protections (e.g., IRB requirements, confidentiality standards). Excellent time management ...
Knowledge of scientific integrity principles, responsible conduct of research, and human subject protections (e.g., IRB requirements, confidentiality standards). Excellent time management ...
... IRB and sponsor guidelines. * Identifies and recruits patients into study protocols as needed ... Is responsible for managing the study documentation and data collection for the study, and ...
... IRB and sponsor guidelines. * Identifies and recruits patients into study protocols as needed ... Is responsible for managing the study documentation and data collection for the study, and ...
Manages all phases of complex research projects with the PI * Works directly with the principal ... Prepare research documents, including IRB/data use agreements Required Qualifications* Research ...
Manages all phases of complex research projects with the PI * Works directly with the principal ... Prepare research documents, including IRB/data use agreements Required Qualifications* Research ...
... IRB and sponsor guidelines. * Identifies and recruits patients into study protocols as needed ... Is responsible for managing the study documentation and data collection for the study, and ...
... IRB and sponsor guidelines. * Identifies and recruits patients into study protocols as needed ... Is responsible for managing the study documentation and data collection for the study, and ...
Psychologist (Education Debt Repayment and Sign on Bonus)
Battle Creek, MI · On-site +1
$120K - $157K/yr
... managing chronic or terminal illness and assisting in or developing new therapy groups and ... Any VACO protocols will have been preapproved by a national IRB and can be implemented as soon as ...
Psychologist (Education Debt Repayment and Sign on Bonus)
Battle Creek, MI · On-site +1
$120K - $157K/yr
... managing chronic or terminal illness and assisting in or developing new therapy groups and ... Any VACO protocols will have been preapproved by a national IRB and can be implemented as soon as ...
Contributes to training tools, supports IRB submissions, and helps transition newly activated ... Maintain clear and complete documentation of the startup process in CTMS and trial management ...
Contributes to training tools, supports IRB submissions, and helps transition newly activated ... Maintain clear and complete documentation of the startup process in CTMS and trial management ...
Contributes to training tools, supports IRB submissions, and helps transition newly activated ... Maintain clear and complete documentation of the startup process in CTMS and trial management ...
Contributes to training tools, supports IRB submissions, and helps transition newly activated ... Maintain clear and complete documentation of the startup process in CTMS and trial management ...
WOC- Research Health Technician
Detroit, MI · On-site +1
$17.75 - $24.50/hr
... management. Major Duties : * Clinical research coordination experience, knowledge of Good Clinical Practice (GCP), IRB and VA research requirements. * Recruitment and regulatory documentation, and ...
WOC- Research Health Technician
Detroit, MI · On-site +1
$17.75 - $24.50/hr
... management. Major Duties : * Clinical research coordination experience, knowledge of Good Clinical Practice (GCP), IRB and VA research requirements. * Recruitment and regulatory documentation, and ...
Irb Manager information
See Michigan salary details
$51K - $54.2K
6% of jobs
$54.2K - $57.5K
7% of jobs
$57.5K - $60.7K
2% of jobs
$60.7K - $64K
6% of jobs
$65K is the 25th percentile. Wages below this are outliers.
$64K - $67.2K
9% of jobs
The median wage is $68.7K / yr.
$67.2K - $70.5K
40% of jobs
$71K is the 75th percentile. Wages above this are outliers.
$70.5K - $73.7K
20% of jobs
$73.7K - $77K
6% of jobs
$77K - $80.2K
1% of jobs
$80.2K - $83.5K
0% of jobs
$83.5K - $86.7K
1% of jobs
$51K
$68.5K
$86.7K
How much do irb manager jobs pay per year?
As of Aug 18, 2026, the average yearly pay for irb manager in Michigan is $68,499.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,400.00 and $71,000.00 per year, depending on experience, location, and employer.
What is an IRB manager?
An IRB (Institutional Review Board) Manager oversees the ethical review process for research involving human subjects, ensuring compliance with federal regulations and institutional policies. They coordinate IRB meetings, review study protocols, and assist researchers in navigating the approval process. The role involves training staff, maintaining records, and staying updated on regulatory changes to protect human research participants.
What are the key skills and qualifications needed to thrive as an IRB manager?
To thrive as an IRB Manager, you need expertise in research ethics, regulatory compliance, and protocol review, often supported by a bachelor’s or master’s degree in a related field and experience with Institutional Review Boards. Familiarity with electronic IRB management systems (such as IRBNet or iMedRIS) and professional certifications like CIP (Certified IRB Professional) are also beneficial. Strong organizational skills, attention to detail, and effective communication help facilitate collaboration with researchers and regulatory bodies. These competencies ensure ethical research practices and efficient, compliant review processes within institutions.
What are some common challenges faced by IRB managers in their daily work?
IRB Managers frequently navigate the complex and evolving landscape of federal, state, and institutional regulations governing human subjects research, which can be both challenging and rewarding. They must balance thorough protocol reviews with timely decision-making, ensuring research projects start on schedule while safeguarding participant welfare. Managing communication between researchers, IRB members, and compliance officers requires strong organizational skills and diplomacy. These challenges make the role dynamic and integral to maintaining the integrity of research within the institution.
What are the most commonly searched types of Irb jobs in Michigan?
The most popular types of Irb jobs in Michigan are:
What are popular job titles related to Irb Manager jobs in Michigan?
For Irb Manager jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Irb Manager jobs in Michigan look for?
The top searched job categories for Irb Manager jobs in Michigan are:
What cities in Michigan are hiring for Irb Manager jobs?
Cities in Michigan with the most Irb Manager job openings:
Full-time
Medical, Dental, Vision, Retirement
Posted 13 days ago
University Of Michigan rating
8.1
Based on 145 frontline employees who took The Breakroom Quiz
162nd of 618 rated colleges and universities
Job description
How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Mission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
Job Summary
The Project Manager provides comprehensive operational leadership for a multidisciplinary vision research program within the Department of Ophthalmology and Visual Sciences. This position oversees complex research studies focused on diabetic eye disease and vision science, manages an internationally utilized ocular tissue biorepository, coordinates collaborations with academic institutions, industry partners, eye banks, and investigators, and ensures regulatory compliance throughout the research lifecycle. The successful candidate serves as the central operational liaison among investigators, research staff, external collaborators, and institutional offices while supporting the continued growth of innovative translational research initiatives.
Responsibilities*
Lead day-to-day management of multiple complex research projects from initiation through closeout.
Coordinate project timelines, milestones, budgets, deliverables, and sponsor reporting requirements.
Manage operations for a nationally and internationally utilized ocular tissue biorepository.
Coordinate procurement, processing, tracking, storage, and distribution of human biospecimens.
Facilitate collaborations with academic institutions, industry partners, eye banks, and external investigators.
Develop and maintain project documentation, standard operating procedures (SOPs), study trackers, and operational workflows.
Monitor compliance with institutional policies, Good Clinical Practice (GCP), HIPAA, and sponsor requirements.
Coordinate Material Transfer Agreements (MTAs), Data Use Agreements (DUAs), research contracts, and collaborator onboarding.
Prepare scientific progress reports and project updates for investigators, sponsors, and collaborators.
Facilitate multidisciplinary meetings and communicate project status to investigators and leadership.
Maintain research databases and ensure high-quality data management practices.
Identify operational risks and implement mitigation strategies to maintain project timelines.
Train and supervise research personnel on project operations and regulatory requirements.
Support strategic planning and expansion of collaborative research initiatives.
Required Qualifications*
Bachelor's degree in Public Health, Biological Sciences, Health Sciences, or a related field.
Five or more years of progressively responsible experience in clinical research, translational research, or research administration.
Demonstrated experience managing multiple complex research projects simultaneously.
Excellent organizational, communication, and problem-solving skills.
Experience developing project timelines and coordinating multidisciplinary teams.
Proficiency with Microsoft Office Suite and research database management.
Ability to work independently while collaborating effectively with investigators, team-members and external partners.
Desired Qualifications*
Master's degree (MPH, MHA, MS, MBA, or related discipline).
PMP, CCRP, CCRC, or other professional project management or clinical research certification.
Experience managing foundation-funded, industry-sponsored, or investigator-initiated research.
Experience supporting biospecimen repositories or translational research programs.
Experience with human subjects research regulations and IRB submissions.
Knowledge of MTAs, DUAs, research contracts, and collaborative research agreements.
Experience supervising or mentoring research personnel.
Experience supporting multicenter or international research collaborations.
Familiarity with ophthalmology, diabetes research, vision science, or biomedical research operations.
Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
What Benefits can you Look Forward to?
Modes of Work
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes .
Background Screening
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.
U-M EEO Statement
The University of Michigan is an Equal Opportunity Employer. We are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities.
Job Detail
Job Opening ID
281251
Working Title
Project Associate Manager
Job Title
Project Associate Manager
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Hybrid
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Ophthal. & Visual Science
Posting Begin/End Date
8/05/2026 - 8/19/2026
Career Interest
Administration
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Mission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
Job Summary
The Project Manager provides comprehensive operational leadership for a multidisciplinary vision research program within the Department of Ophthalmology and Visual Sciences. This position oversees complex research studies focused on diabetic eye disease and vision science, manages an internationally utilized ocular tissue biorepository, coordinates collaborations with academic institutions, industry partners, eye banks, and investigators, and ensures regulatory compliance throughout the research lifecycle. The successful candidate serves as the central operational liaison among investigators, research staff, external collaborators, and institutional offices while supporting the continued growth of innovative translational research initiatives.
Responsibilities*
Lead day-to-day management of multiple complex research projects from initiation through closeout.
Coordinate project timelines, milestones, budgets, deliverables, and sponsor reporting requirements.
Manage operations for a nationally and internationally utilized ocular tissue biorepository.
Coordinate procurement, processing, tracking, storage, and distribution of human biospecimens.
Facilitate collaborations with academic institutions, industry partners, eye banks, and external investigators.
Develop and maintain project documentation, standard operating procedures (SOPs), study trackers, and operational workflows.
Monitor compliance with institutional policies, Good Clinical Practice (GCP), HIPAA, and sponsor requirements.
Coordinate Material Transfer Agreements (MTAs), Data Use Agreements (DUAs), research contracts, and collaborator onboarding.
Prepare scientific progress reports and project updates for investigators, sponsors, and collaborators.
Facilitate multidisciplinary meetings and communicate project status to investigators and leadership.
Maintain research databases and ensure high-quality data management practices.
Identify operational risks and implement mitigation strategies to maintain project timelines.
Train and supervise research personnel on project operations and regulatory requirements.
Support strategic planning and expansion of collaborative research initiatives.
Required Qualifications*
Bachelor's degree in Public Health, Biological Sciences, Health Sciences, or a related field.
Five or more years of progressively responsible experience in clinical research, translational research, or research administration.
Demonstrated experience managing multiple complex research projects simultaneously.
Excellent organizational, communication, and problem-solving skills.
Experience developing project timelines and coordinating multidisciplinary teams.
Proficiency with Microsoft Office Suite and research database management.
Ability to work independently while collaborating effectively with investigators, team-members and external partners.
Desired Qualifications*
Master's degree (MPH, MHA, MS, MBA, or related discipline).
PMP, CCRP, CCRC, or other professional project management or clinical research certification.
Experience managing foundation-funded, industry-sponsored, or investigator-initiated research.
Experience supporting biospecimen repositories or translational research programs.
Experience with human subjects research regulations and IRB submissions.
Knowledge of MTAs, DUAs, research contracts, and collaborative research agreements.
Experience supervising or mentoring research personnel.
Experience supporting multicenter or international research collaborations.
Familiarity with ophthalmology, diabetes research, vision science, or biomedical research operations.
Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
What Benefits can you Look Forward to?
- Excellent medical, dental and vision coverage effective on your very first day
- 2:1 Match on retirement savings
Modes of Work
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes .
Background Screening
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.
U-M EEO Statement
The University of Michigan is an Equal Opportunity Employer. We are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities.
Job Detail
Job Opening ID
281251
Working Title
Project Associate Manager
Job Title
Project Associate Manager
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Hybrid
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Ophthal. & Visual Science
Posting Begin/End Date
8/05/2026 - 8/19/2026
Career Interest
Administration
What University Of Michigan employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About University of Michigan
Sourced by ZipRecruiter
The University of Michigan (U-M), based in Ann Arbor, MI, US, is one of America's most esteemed institutions in higher education. Established in 1817, it presides in the industry of education and research, providing a range of services including undergraduate, graduate, and professional education programs. Complementing this is an extensive research activity that has significantly contributed to various fields, from healthcare to engineering, humanities to sports. Upholding its mission "to serve the people of Michigan and the world through preeminence in creating, communicating, preserving and applying knowledge, art, and academic values", U-M consistently ranks among the top universities globally, a testament to its tradition of excellence in learning and research, and a deep commitment to innovation and discovery.
Industry
Colleges, universities, and professional schools
Company size
10,000+ Employees
Headquarters location
Ann Arbor, MI, US
Year founded
1817