Proficiency with data management platforms for the submission of Case Report Forms, electronic IRB submission portals, and safety reporting. * Audit Readiness and Post Approval Monitoring: Direct ...
Proficiency with data management platforms for the submission of Case Report Forms, electronic IRB submission portals, and safety reporting. * Audit Readiness and Post Approval Monitoring: Direct ...
Experience managing Institutional Review Board (IRB) regulatory requirements. Experience in study protocols and design. Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, Adobe Acrobat.
Experience managing Institutional Review Board (IRB) regulatory requirements. Experience in study protocols and design. Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, Adobe Acrobat.
Experience managing Institutional Review Board (IRB) regulatory requirements. Experience in study protocols and design. Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, Adobe Acrobat.
Experience managing Institutional Review Board (IRB) regulatory requirements. Experience in study protocols and design. Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, Adobe Acrobat.
... managing Institutional Review Board (IRB) regulatory requirements. • Experience in study protocols and design. • Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, Adobe Acrobat.
... managing Institutional Review Board (IRB) regulatory requirements. • Experience in study protocols and design. • Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook, Adobe Acrobat.
Senior Clinical Research Coordinator
$22.75 - $30.50/hr
Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research ... Completes all protocol-related training and adheres to IRB approved protocol(s) * Support the ...
New
Senior Clinical Research Coordinator
$22.75 - $30.50/hr
Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research ... Completes all protocol-related training and adheres to IRB approved protocol(s) * Support the ...
New
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
... providing management and oversight for research studies from beginning to end of project. This ... Tracks and ensures IRB/IACUC compliance for facility users * Prepares documents for investigator ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Follows study participants; manages collection of data including maintaining records of patient ... Assists in the preparation of periodic and special reports, including reports to IRB-01, Protocol ...
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Works with coordinators in developing/writing IRB applications and other regulatory requirements ...
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Works with coordinators in developing/writing IRB applications and other regulatory requirements ...
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Works with coordinators in developing/writing IRB applications and other regulatory requirements ...
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Works with coordinators in developing/writing IRB applications and other regulatory requirements ...
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Develops/writes IRB applications and other regulatory requirements for research protocols
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Develops/writes IRB applications and other regulatory requirements for research protocols
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Develops/writes IRB applications and other regulatory requirements for research protocols
New
Manages all aspects of the research program in the Division of Neonatology at Stead Family ... Develops/writes IRB applications and other regulatory requirements for research protocols
New
Director of Data Analytics and Governance
Calmar, IA · On-site
$13/hr
Manage the College's Edify data warehouse and associated data lake/reporting infrastructure ... Provide administrative oversight for the Institutional Review Board (IRB) to ensure all research ...
Director of Data Analytics and Governance
Calmar, IA · On-site
$13/hr
Manage the College's Edify data warehouse and associated data lake/reporting infrastructure ... Provide administrative oversight for the Institutional Review Board (IRB) to ensure all research ...
Communicate with IRB staff and investigators. Human Resources/Leadership: * May hire, develop and manage the performance of staff; assure staff is complaint with UI policies and procedures. Financial ...
Communicate with IRB staff and investigators. Human Resources/Leadership: * May hire, develop and manage the performance of staff; assure staff is complaint with UI policies and procedures. Financial ...
Communicate with IRB staff and investigators. Human Resources/Leadership: * May hire, develop and manage the performance of staff; assure staff is complaint with UI policies and procedures. Financial ...
Communicate with IRB staff and investigators. Human Resources/Leadership: * May hire, develop and manage the performance of staff; assure staff is complaint with UI policies and procedures. Financial ...
Irb Manager information
See Iowa salary details
$54.9K - $58.4K
6% of jobs
$58.4K - $61.9K
7% of jobs
$61.9K - $65.4K
2% of jobs
$65.4K - $69K
6% of jobs
$70K is the 25th percentile. Wages below this are outliers.
$69K - $72.5K
9% of jobs
The median wage is $74.1K / yr.
$72.5K - $76K
40% of jobs
$76.6K is the 75th percentile. Wages above this are outliers.
$76K - $79.5K
20% of jobs
$79.5K - $83K
6% of jobs
$83K - $86.5K
1% of jobs
$86.5K - $90K
0% of jobs
$90K - $93.5K
1% of jobs
$54.9K
$73.8K
$93.5K
How much do irb manager jobs pay per year?
As of Aug 14, 2026, the average yearly pay for irb manager in Iowa is $73,818.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,400.00 and $76,600.00 per year, depending on experience, location, and employer.
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 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.
How to become an IRB manager?
To become an IRB manager, candidates typically need a bachelor's degree in a health-related or research field, with many roles preferring a master's degree or higher. Relevant experience in research administration, ethics review, or regulatory compliance is essential, along with strong organizational and leadership skills. Certifications such as the Certified IRB Professional (CIP) can enhance qualifications for this role.
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 most commonly searched types of Irb jobs in Iowa?
The most popular types of Irb jobs in Iowa are:
What are popular job titles related to Irb Manager jobs in Iowa?
For Irb Manager jobs in Iowa, the most frequently searched job titles are:
What job categories do people searching Irb Manager jobs in Iowa look for?
The top searched job categories for Irb Manager jobs in Iowa are:
ThedaCare rating
6.6
Based on 128 frontline employees who took The Breakroom Quiz
570th of 887 rated healthcare providers
Job description
Why ThedaCare?
Living A Life Inspired!
Our new vision at ThedaCare is bold, ambitious, and ignited by a shared passion to provide outstanding care. We are inspired to reinvent health care by becoming a proactive partner in health, enriching the lives of all and creating value in everything we do. Each of us are called to take action in delivering higher standards of care, lower costs and a healthier future for our patients, our families, our communities and our world.
At ThedaCare, our team members are empowered to be the catalyst of change through our values of compassion, excellence, leadership, innovation, and agility. A career means much more than excellent compensation and benefits. Our team members are supported by continued opportunities for learning and development, accessible and transparent leadership, and a commitment to work/life balance. If you're interested in joining a health care system that is changing the face of care and well-being in our community, we encourage you to explore a future with ThedaCare.
Benefits, with a whole-person approach to wellness -
- Lifestyle Engagement
- e.g. health coaches, relaxation rooms, health focused apps (Wonder, Ripple), mental health support
- Access & Affordability
- e.g. minimal or zero copays, team member cost sharing premiums, daycare
About ThedaCare!
Summary :The Research Regulatory Coordinator manages compliance, documentation, and submissions for clinical trials and human subject's research. This role acts as the primary liaison between clinical investigators, institutional review boards (IRBs), and study sponsors. The ideal candidate will ensure all research activities strictly adhere to federal, state, and institutional guidelines.Job Description:Essential Duties and Responsibilities
- IRB Submissions: Prepare, submit, and track initial protocols, amendments, continuing reviews, and safety reports to the IRB.
- Regulatory Documentation: Maintains organized records of all regulatory submission, approvals, and correspondence with regulatory bodies; maintains master regulatory binders (paper and electronic) ensuring audit-ready status at all times.
- Study Startup: Coordinate the collection, maintenance and storage of essential documents, including investigator CVs, medical licenses, financial disclosure forms, and organization required trainings.
- Compliance Monitoring: Maintain knowledge of current federal, state, and organizational regulations, guidelines, and industry standards related to research and ensures research activities comply with federal, state, and organizational regulations related to human subject research.
- Protocol Review & Study Tracking: Assist in the review of research protocols to ensure compliance with regulatory standards. Monitors study timelines as outlined with the sponsor and protocol.
- Trains & Supports: Acts as a resource for researchers, research office staff, learners and residents regarding regulatory process and documentation standards.
- Communicates & Works Collaboratively: Serves as the central point of contact for researchers, sponsors, contract research organizations (CROs), IRB, regulatory bodies and stakeholders.
- Audit & Monitor Visit Preparation: Assist with internal quality assurance audits, post approval monitoring and external inspections by federal agencies or sponsors.
Required Qualifications
- Education: Bachelor's degree in healthcare administration, life sciences, public health, or a related field.
- Experience: Minimum of 2 years of direct experience in clinical research, research regulatory affairs or IRB administration.
- Knowledge: Strong understanding of FDA regulations, HHS human subject protections (45 CFR 46), and ICH/GCP guidelines.
Preferred Qualifications
- One or more of the following preferred and/or able to obtain within 6 months of hire: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP), or Certified Institutional Review Board Professional (CIP).
- Technology: Proficiency with data management platforms for the submission of Case Report Forms, electronic IRB submission portals, and safety reporting.
- Audit Readiness and Post Approval Monitoring: Direct experience preparing for and participating in successful FDA audits, sponsor inspections, post-approval monitoring or quality assurance audits and site visits.
What ThedaCare employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About ThedaCare
Sourced by ZipRecruiter
We want to make exceptional care effortless for our patients. At ThedaCare, that means going above and beyond treating a particular condition – it means helping you achieve better health for life. You and your family are at the center of everything we do, from prioritizing your schedule when making appointments to designing our facilities for your comfort and convenience. Remaining proactive in your care allows us to better predict and prevent disease before complications arise, and when it comes to making important health-related decisions, we are here to support you. In every interaction, we want you to have full confidence the care you receive is purposeful, cost-effective and will help you continue enjoying life as you’ve planned it. ThedaCare is the third largest healthcare employer in Wisconsin, and the largest employer in Northeast Wisconsin with over 7,000 team members.
Industry
Health care and social assistance
Company size
5,001 - 10,000 Employees
Headquarters location
Neenah, WI, US
Year founded
1909