IRB Analyst
Grand Rapids, MI · Hybrid
Relevant program/project management experience * CRT-IRB Professional, Certified (CIP) About Corewell Health As a team member at Corewell Health, you will play an essential role in delivering ...
New
Grand Rapids, MI · Hybrid
Relevant program/project management experience * CRT-IRB Professional, Certified (CIP) About Corewell Health As a team member at Corewell Health, you will play an essential role in delivering ...
New
Grand Rapids, MI · Hybrid
Relevant program/project management experience * CRT-IRB Professional, Certified (CIP) About Corewell Health As a team member at Corewell Health, you will play an essential role in delivering ...
New
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Strong organizational and project management skills. * Ability to lead change and foster ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Strong organizational and project management skills. * Ability to lead change and foster ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Strong organizational and project management skills. * Ability to lead change and foster ...
Assistin developing research protocols, IRB submissions, and regulatory documentation ... Strong organizational and project management skills. * Ability to lead change and foster ...
Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation ... Strong organizational and project management skills. * Ability to lead change and foster ...
Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation ... Strong organizational and project management skills. * Ability to lead change and foster ...
Work with others on IRB submissions and amendments. o Ensure all data collection methods strictly ... Staff Management: Assist others in hiring, training, and supervising survey research staff ...
Work with others on IRB submissions and amendments. o Ensure all data collection methods strictly ... Staff Management: Assist others in hiring, training, and supervising survey research staff ...
... IRB processes, and site management • Experience with budgets, contracts, and regulatory and quality workflows • Excellent communication, leadership, and problem-solving skills
... IRB processes, and site management • Experience with budgets, contracts, and regulatory and quality workflows • Excellent communication, leadership, and problem-solving skills
... IRB processes, and site management • Experience with budgets, contracts, and regulatory and quality workflows • Excellent communication, leadership, and problem-solving skills
... IRB processes, and site management • Experience with budgets, contracts, and regulatory and quality workflows • Excellent communication, leadership, and problem-solving skills
Flint, MI · On-site
$140 - $190/hr
Strong knowledge of GCP, FDA regulations, IRB processes, and site management * Experience with budgets, contracts, and regulatory and quality workflows * Excellent communication, leadership, and ...
Flint, MI · On-site
$140 - $190/hr
Strong knowledge of GCP, FDA regulations, IRB processes, and site management * Experience with budgets, contracts, and regulatory and quality workflows * Excellent communication, leadership, and ...
Work with others on IRB submissions and amendments. o Ensure all data collection methods strictly ... Strong organizational and time-management skills. • Effectively utilize software necessary to ...
Work with others on IRB submissions and amendments. o Ensure all data collection methods strictly ... Strong organizational and time-management skills. • Effectively utilize software necessary to ...
Detroit, MI · On-site
Assures IRB approval is obtained prior to initiation of studies. In collaboration with study ... management experience in a health care research setting. Facility Statement The Detroit Medical ...
Detroit, MI · On-site
Assures IRB approval is obtained prior to initiation of studies. In collaboration with study ... management experience in a health care research setting. Facility Statement The Detroit Medical ...
Ann Arbor, MI · On-site
$95 - $140/hr
Manage IRB submissions, regulatory documentation, and clinical trial compliance in accordance with federal regulations, institutional policies, and sponsor requirements (GCP/ICH). * Supervise, mentor ...
Ann Arbor, MI · On-site
$95 - $140/hr
Manage IRB submissions, regulatory documentation, and clinical trial compliance in accordance with federal regulations, institutional policies, and sponsor requirements (GCP/ICH). * Supervise, mentor ...
Detroit, MI · On-site
$19 - $26.25/hr
Knowledge of scientific integrity principles, responsible conduct of research, and human subject protections (e.g., IRB requirements, confidentiality standards). Excellent time management ...
Detroit, MI · On-site
$19 - $26.25/hr
Knowledge of scientific integrity principles, responsible conduct of research, and human subject protections (e.g., IRB requirements, confidentiality standards). Excellent time management ...
Detroit, MI · On-site
$19 - $26.25/hr
Implement IRB applications and amendments. Coordinating human MRI scans. Proofread and edit research data and documents to ensure accuracy. Management of pre- and post-awards. Perform other related ...
Detroit, MI · On-site
$19 - $26.25/hr
Implement IRB applications and amendments. Coordinating human MRI scans. Proofread and edit research data and documents to ensure accuracy. Management of pre- and post-awards. Perform other related ...
$24 - $32/hr
... research management organization in the Houston area and one of the top 50 in the country, is ... Sponsor provided and IRB approved protocol b. All amendments c. Investigator Brochure d. Sponsor ...
$24 - $32/hr
... research management organization in the Houston area and one of the top 50 in the country, is ... Sponsor provided and IRB approved protocol b. All amendments c. Investigator Brochure d. Sponsor ...
This position is responsible for the submission and management of Institutional Review Board (IRB) applications and annual renewals, preparation of study files as well as data acquisition and study ...
New
This position is responsible for the submission and management of Institutional Review Board (IRB) applications and annual renewals, preparation of study files as well as data acquisition and study ...
New
Detroit, MI · On-site
Assures IRB approval is obtained prior to initiation of studies. In collaboration with study ... management experience in a health care research setting. Facility Statement The Detroit Medical ...
Detroit, MI · On-site
Assures IRB approval is obtained prior to initiation of studies. In collaboration with study ... management experience in a health care research setting. Facility Statement The Detroit Medical ...
IRB, FDA, and clinical trial requirements * Laboratory safety and quality standards * Support ... Process & Stakeholder Management * Collaborate with HR and Talent Acquisition on candidate ...
IRB, FDA, and clinical trial requirements * Laboratory safety and quality standards * Support ... Process & Stakeholder Management * Collaborate with HR and Talent Acquisition on candidate ...
$24 - $32/hr
Sponsor-provided and IRB-approved Protocol Training * All relevant Protocol Amendments Training ... Any other matters as assigned by management. Knowledge amp; Experience: Education: * High School ...
$24 - $32/hr
Sponsor-provided and IRB-approved Protocol Training * All relevant Protocol Amendments Training ... Any other matters as assigned by management. Knowledge amp; Experience: Education: * High School ...
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 ...
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 ...
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 ...
$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
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.
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.
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.
The most popular types of Irb jobs in Michigan are:
For Irb Manager jobs in Michigan, the most frequently searched job titles are:
The top searched job categories for Irb Manager jobs in Michigan are:
Cities in Michigan with the most Irb Manager job openings:

Full-time
Medical, Vision, Retirement
Posted 2 days ago
New
Responsible for all activities in support of the Human Research Protection Program (HRPP) by facilitating and participating in the regulatory review of human subject's research conducted under the jurisdiction of the Corewell Health HRPP. Provides regulatory support and oversight for the Research Community and serves as a point of contact for submission inquiries and requests for guidance and consultation as it pertains to the federal regulations, state and local laws, as well as Corewell Health Policies governing human subjects research. Ensures that Corewell Health's human research activities are conducted in compliance with institutional standard operating procedures (SOPs) and international, federal, state, and local rules and regulations and ethical principles regarding human subject research. May serve as an official member of the Institutional Review Board (IRB) Committee and/or a "designated" reviewer, as applicable.
Essential FunctionsRequired
Preferred
As a team member at Corewell Health, you will play an essential role in delivering personalized health care to our patients, members and our communities. We are committed to cultivating and investing in YOU. Our top-notch teams are comprised of collaborators, leaders and innovators that continue to build on one shared mission statement - to improve health, instill humanity and inspire hope. Join a nationally recognized health system with an ambitious vision of continued advancement and excellence.
Primary Location
SITE - Secchia Center - 15 Michigan St NE - Grand RapidsDepartment Name
Sponsored Programs Instiutional Review Board - Grand Rapids HospEmployment Type
Full timeShift
Day (United States of America)Weekly Scheduled Hours
40Hours of Work
9:00 a.m. - 5:00 p.m.Days Worked
Monday to FridayWeekend Frequency
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Corewell Health is committed to providing a safe environment for our team members, patients, visitors, and community. We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site or hybrid workplace category. We are committed to supporting prospective team members who require reasonable accommodations to participate in the job application process, to perform the essential functions of a job, or to enjoy equal benefits and privileges of employment due to a disability, pregnancy, or sincerely held religious belief.
Corewell Health grants equal employment opportunity to all qualified persons without regard to race, color, national origin, sex, disability, age, religion, genetic information, marital status, height, weight, gender, pregnancy, sexual orientation, gender identity or expression, veteran status, or any other legally protected category.
An interconnected, collaborative culture where all are encouraged to bring their whole selves to work, is vital to the health of our organization. As a health system, we advocate for equity as we care for our patients, our communities, and each other. From workshops that develop cultural intelligence, to our inclusion resource groups for people to find community and empowerment at work, we are dedicated to ongoing resources that advance our values of diversity, equity, and inclusion in all that we do. We invite those that share in our commitment to join our team.
You may request assistance in completing the application process by calling 616.486.7447.