Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings. Our Commitment ...
Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings. Our Commitment ...
Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings. Rooted in our ...
Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings. Rooted in our ...
Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings. Our Commitment ...
Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings. Our Commitment ...
... FQ submissions, IRB submissions, amendments, and reporting • Support contract and budget negotiations, including feasibility review and cost analysis • Ensure quality standards across ...
... FQ submissions, IRB submissions, amendments, and reporting • Support contract and budget negotiations, including feasibility review and cost analysis • Ensure quality standards across ...
... FQ submissions, IRB submissions, amendments, and reporting • Support contract and budget negotiations, including feasibility review and cost analysis • Ensure quality standards across ...
... FQ submissions, IRB submissions, amendments, and reporting • Support contract and budget negotiations, including feasibility review and cost analysis • Ensure quality standards across ...
Associate Director Research Operations
Flint, MI · 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 ...
Associate Director Research Operations
Flint, MI · 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 ...
This position manages and develops the Data Team of Research Associates and Research Assistants, directs all Institutional Review Board (IRB) Submissions and Regulatory and Compliance matters, and ...
New
This position manages and develops the Data Team of Research Associates and Research Assistants, directs all Institutional Review Board (IRB) Submissions and Regulatory and Compliance matters, and ...
New
Research Compliance Quality Improvement Education Specialist - HYBRID - Part Time
Grand Blanc, MI · 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.
Research Compliance Quality Improvement Education Specialist - HYBRID - Part Time
Grand Blanc, MI · 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.
Research Compliance Quality Improvement Education Specialist - HYBRID - Part Time
Grand Blanc, MI · 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.
Research Compliance Quality Improvement Education Specialist - HYBRID - Part Time
Grand Blanc, MI · 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.
Coordinator Clinical Research
Flint, MI · 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 ...
Coordinator Clinical Research
Flint, MI · 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.
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.
Research Compliance Quality Improvement Education Specialist - HYBRID - Part Time
Grand Blanc, MI · 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.
Research Compliance Quality Improvement Education Specialist - HYBRID - Part Time
Grand Blanc, MI · 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.
Coordinator Clinical Research
Flint, MI · 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 ...
Coordinator Clinical Research
Flint, MI · 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 ...
Coordinator Clinical Research
Flint, MI · 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 ...
Coordinator Clinical Research
Flint, MI · 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 ...
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 ...
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 ...
Research Assistant, Population Sciences - Department of Oncology
Detroit, MI · On-site
$19 - $26.25/hr
Conduct study visits and collect clinical and research data in compliance with Institutional Review Board (IRB), regulatory, and protocol requirements. Communicate regularly with the Principal ...
Research Assistant, Population Sciences - Department of Oncology
Detroit, MI · On-site
$19 - $26.25/hr
Conduct study visits and collect clinical and research data in compliance with Institutional Review Board (IRB), regulatory, and protocol requirements. Communicate regularly with the Principal ...
Irb information
What does an IRB analyst do?
An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements. They evaluate risks, consent processes, and study procedures, often working with institutional review boards to approve or modify research proposals. Strong attention to detail and knowledge of federal regulations are essential for this role.
What are the key skills and qualifications needed to thrive as an IRB administrator, and why are they important?
To thrive as an IRB Administrator, you need expertise in research ethics, regulatory compliance, and human subject protection, usually supported by a relevant bachelor's or master's degree. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are typically required. Strong organizational skills, attention to detail, and effective communication are crucial for coordinating reviews and guiding researchers. These skills ensure ethical research practices, regulatory compliance, and the protection of research participants.
What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?
An IRB (Institutional Review Board) coordinator is responsible for managing the review process of research protocols involving human subjects to ensure compliance with ethical standards and federal regulations. This role involves working closely with researchers to guide them through the submission process, reviewing applications for completeness, and facilitating communication between the IRB committee and research teams. Coordinators also serve as liaisons with regulatory bodies, maintain records, and help organize IRB meetings. Strong organizational, communication, and regulatory knowledge are essential, as coordinators often balance multiple projects and deadlines while ensuring research integrity and participant safety.
How to get an IRB job?
To get an IRB (Institutional Review Board) job, candidates typically need a background in research ethics, healthcare, or related fields, along with relevant experience. Certifications such as the CITI Program Human Subjects Research course can be beneficial, and strong knowledge of regulatory requirements like 45 CFR 46 is often required. Positions may require a bachelor's or higher degree and attention to detail in reviewing research protocols.
What is an IRB?
An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects. The primary purpose of the IRB is to ensure that the rights, welfare, and privacy of participants are protected throughout the research process. IRBs review research proposals to ensure ethical standards are met and that risks to participants are minimized. They are required for most research conducted at universities, hospitals, and other organizations that receive federal funding.
What is the difference between Irb vs Clinical Research Coordinator?
| 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.
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 jobs in Michigan? For Irb jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Irb jobs in Michigan look for? The top searched job categories for Irb jobs in Michigan are:
- Online Clinical Research
- Temporary Clinical Trials Test Subject
- Manager Clinical Research Informatics
- Medical Device Clinical Research Manager
- Director Gsk Clinical Research
- Clinical Research Data Manager
- Clinical Research Project Manager
- Biomedical Research Assistant
- Overnight Clinical Research Coordinator
- Clinical Trials Director
What cities in Michigan are hiring for Irb jobs? Cities in Michigan with the most Irb job openings:
Full-time
Posted 25 days ago
Trinity Health rating
6.6
Based on 354 frontline employees who took The Breakroom Quiz
572nd of 887 rated healthcare providers
Job description
Employment Type:
Full timeShift:
Day Shift
Description:
Position summary:
Performs all duties necessary to review, implement, coordinate, manage and monitor oncology research activities at Trinity Health Grand Rapids Hospital. Also provides occasional support and/or coverage at Trinity Health Muskegon and the Johnson Family Cancer Center. This includes screening and recruitment of eligible patients through collaboration with oncology providers and other engaged community oncology programs. Additionally, these responsibilities extend to clinical trial opportunities provided by external pharmaceutical and industry sponsors and specific to the oncology patient population.
Minimum qualifications:
What the Oncology Research RN Coordinator will do:
Our Commitment
Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.
Full timeShift:
Day Shift
Description:
Position summary:
Performs all duties necessary to review, implement, coordinate, manage and monitor oncology research activities at Trinity Health Grand Rapids Hospital. Also provides occasional support and/or coverage at Trinity Health Muskegon and the Johnson Family Cancer Center. This includes screening and recruitment of eligible patients through collaboration with oncology providers and other engaged community oncology programs. Additionally, these responsibilities extend to clinical trial opportunities provided by external pharmaceutical and industry sponsors and specific to the oncology patient population.
Minimum qualifications:
- Graduate of an accredited school of nursing
- BSN and Oncology Nurse Certification preferred
- Current Michigan RN license
- Minimum of 2 years' experience in an acute Oncology care setting
- Strong knowledge of Microsoft Office and EPIC EMR platform as well as computer skills necessary to navigate clinical research data platforms
What the Oncology Research RN Coordinator will do:
- Assumes responsibilities for the review, implementation, coordination, and management of all oncology research activities performed at Trinity Health West Michigan sites.
- Coordinates and maintains all regulatory documents and investigative site files necessary to achieve compliance with the FDA, OHRP, Trinity Health Research Compliance, Trinity Health Regional Institutional Review Board or applicable central IRB, as well as sponsoring entities.
- Serves as a liaison between oncologists, radiation oncologists, pharmacists, nurse navigators, mid-level providers and all others involved in the provision of research related care to ensure timely dissemination of information and maintain positive working relationships.
- Develops and facilitates research process and procedure to support cooperation with external oncology research collaborators such as Michigan Cancer Research Consortium, and other future partners.
- Contributes to the implementation of an oncology research scientific review committee.
- Compiles all study related documents for IRB submission, and as applicable, completes the IRB application, attends the IRB meeting, and facilitates resolution of any IRB findings.
Our Commitment
Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.
What Trinity Health employees say
Pay
Benefits
Hours and flexibility
Workplace
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About Trinity Health
Sourced by ZipRecruiter
Trinity Health Ann Arbor is a 537 -bed teaching hospital located on 340 acre campus. Recognized by IBM Watson as a Top 100 Hospital and #1 Teaching Hospital, Trinity Health Ann Arbor has been a leading health care provider for more than 100 years. Trinity Health has received numerous local and national awards in recognition of our leadership, quality outcomes, and clinical excellence.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Livonia, MI, US