IRB Analyst
Grand Rapids, MI ยท Hybrid
Functions as a liaison within and between the IRB committee, investigators and their designees, and other research support staff. * Ensures timely processing, review and disposition of research ...
Grand Rapids, MI ยท Hybrid
Functions as a liaison within and between the IRB committee, investigators and their designees, and other research support staff. * Ensures timely processing, review and disposition of research ...
Grand Rapids, MI ยท Hybrid
Functions as a liaison within and between the IRB committee, investigators and their designees, and other research support staff. * Ensures timely processing, review and disposition of research ...
Grand Rapids, MI ยท On-site
Functions as a liaison within and between the IRB committee, investigators and their designees, and other research support staff. * Ensures timely processing, review and disposition of research ...
Grand Rapids, MI ยท On-site
Functions as a liaison within and between the IRB committee, investigators and their designees, and other research support staff. * Ensures timely processing, review and disposition of research ...
Direct IRB administration experience * Multi-committee exposure (highly valuable at HFH) to IRB + IACUC + IBC/Biosafety familiarity & Understanding of cross-committee coordination and dependencies.
Direct IRB administration experience * Multi-committee exposure (highly valuable at HFH) to IRB + IACUC + IBC/Biosafety familiarity & Understanding of cross-committee coordination and dependencies.
Direct IRB administration experience * Multi-committee exposure (highly valuable at HFH) to IRB + IACUC + IBC/Biosafety familiarity & Understanding of cross-committee coordination and dependencies.
Direct IRB administration experience * Multi-committee exposure (highly valuable at HFH) to IRB + IACUC + IBC/Biosafety familiarity & Understanding of cross-committee coordination and dependencies.
... FQ submissions, IRB submissions, amendments, and reporting โข Support contract and budget negotiations, including feasibility review and cost analysis โข Ensure quality standards across ...
... FQ submissions, IRB submissions, amendments, and reporting โข Support contract and budget negotiations, including feasibility review and cost analysis โข Ensure quality standards across ...
... FQ submissions, IRB submissions, amendments, and reporting โข Support contract and budget negotiations, including feasibility review and cost analysis โข Ensure quality standards across ...
... FQ submissions, IRB submissions, amendments, and reporting โข Support contract and budget negotiations, including feasibility review and cost analysis โข Ensure quality standards across ...
Flint, MI ยท On-site
$140 - $190/hr
Collaborate with Feasibility and start up/regulatory teams to ensure timely FQ submissions, IRB submissions, amendments, and reporting * Support contract and budget negotiations, including ...
Flint, MI ยท On-site
$140 - $190/hr
Collaborate with Feasibility and start up/regulatory teams to ensure timely FQ submissions, IRB submissions, amendments, and reporting * Support contract and budget negotiations, including ...
Regulatory Oversight & IRB Management: Independently author, submit, amend, and maintain complex IRB protocols spanning both industry-sponsored and NIH-funded projects. Ensure strict regulatory ...
New
Regulatory Oversight & IRB Management: Independently author, submit, amend, and maintain complex IRB protocols spanning both industry-sponsored and NIH-funded projects. Ensure strict regulatory ...
New
Grand Blanc, MI ยท On-site
Facilitate the execution of system wide training programs, workshops and conferences for investigators, IRB members and research staff: * Develops and presents monthly education sessions.
Grand Blanc, MI ยท On-site
Facilitate the execution of system wide training programs, workshops and conferences for investigators, IRB members and research staff: * Develops and presents monthly education sessions.
Grand Blanc, MI ยท On-site
Facilitate the execution of system wide training programs, workshops and conferences for investigators, IRB members and research staff: * Develops and presents monthly education sessions.
Grand Blanc, MI ยท On-site
Facilitate the execution of system wide training programs, workshops and conferences for investigators, IRB members and research staff: * Develops and presents monthly education sessions.
Flint, MI ยท On-site
$23.50 - $31.25/hr
Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...
Flint, MI ยท On-site
$23.50 - $31.25/hr
Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...
Assistin developing research protocols, IRB submissions, and regulatory documentation. * Coordinatelogisticsfor research activities including recruitment, data collection, and reporting.
Assistin developing research protocols, IRB submissions, and regulatory documentation. * Coordinatelogisticsfor research activities including recruitment, data collection, and reporting.
Grand Blanc, MI ยท Hybrid
Facilitate the execution of system wide training programs, workshops and conferences for investigators, IRB members and research staff: * Develops and presents monthly education sessions.
Grand Blanc, MI ยท Hybrid
Facilitate the execution of system wide training programs, workshops and conferences for investigators, IRB members and research staff: * Develops and presents monthly education sessions.
Assistin developing research protocols, IRB submissions, and regulatory documentation. * Coordinatelogisticsfor research activities including recruitment, data collection, and reporting.
Assistin developing research protocols, IRB submissions, and regulatory documentation. * Coordinatelogisticsfor research activities including recruitment, data collection, and reporting.
Flint, MI ยท On-site
$23.50 - $31.25/hr
Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...
Flint, MI ยท On-site
$23.50 - $31.25/hr
Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...
Royal Oak, MI ยท On-site
Communicate effectively with the IRB, research participants, research team, principal investigators, sponsors, primary care providers, and ancillary staff to educate on protocol requirements, and to ...
Royal Oak, MI ยท On-site
Communicate effectively with the IRB, research participants, research team, principal investigators, sponsors, primary care providers, and ancillary staff to educate on protocol requirements, and to ...
Flint, MI ยท On-site
$23.50 - $31.25/hr
Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...
Flint, MI ยท On-site
$23.50 - $31.25/hr
Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO. 7. Assists the investigators and clinicians in identifying and ...
Communicate effectively with the IRB, research participants, research team, principal investigators, sponsors, primary care providers, and ancillary staff to educate on protocol requirements, and to ...
Communicate effectively with the IRB, research participants, research team, principal investigators, sponsors, primary care providers, and ancillary staff to educate on protocol requirements, and to ...
Royal Oak, MI ยท On-site
Communicate effectively with the IRB, research participants, research team, principal investigators, sponsors, primary care providers, and ancillary staff to educate on protocol requirements, and to ...
Royal Oak, MI ยท On-site
Communicate effectively with the IRB, research participants, research team, principal investigators, sponsors, primary care providers, and ancillary staff to educate on protocol requirements, and to ...
Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation, dissemination of findings, and evidence-based practice principles. * Support facilitation of ...
Mentor and educate nurses on research methodologies, proposals, IRB submission, data interpretation, dissemination of findings, and evidence-based practice principles. * Support facilitation of ...
| 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 Michigan are:
For Irb jobs in Michigan, the most frequently searched job titles are:
The top searched job categories for Irb jobs in Michigan are:
Cities in Michigan with the most Irb job openings:

Full-time
Medical, Vision, Retirement
Posted 4 days ago
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.