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Irb Analyst Jobs in Minnesota (NOW HIRING)

Performing day-to-day dispensing and accountability activities with regard to IRB-approved clinical ... analysis and submission of required reports. * Updates and improves the department processes and ...

New

AP Research Tutor

Edina, MN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

AP Research Tutor

Saint Paul, MN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

AP Research Tutor

Minneapolis, MN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

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Irb Analyst information

See Minnesota salary details

$30.4K

$71.8K

$127.3K

How much do irb analyst jobs pay per year?

As of Aug 23, 2026, the average yearly pay for irb analyst in Minnesota is $71,753.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,400.00 and $85,200.00 per year, depending on experience, location, and employer.

What is an IRB analyst?

An IRB (Institutional Review Board) Analyst is responsible for reviewing research proposals to ensure they comply with ethical guidelines and regulatory requirements for human subjects' protection. They assess study protocols, verify informed consent procedures, and ensure adherence to federal and institutional policies. IRB Analysts collaborate with researchers to address compliance issues and provide guidance on ethical research practices. Their role is critical in safeguarding participants' rights and welfare while facilitating ethical research.

What are the key skills and qualifications needed to thrive as an IRB analyst?

To thrive as an IRB Analyst, you need a strong background in research ethics, regulatory compliance, and an understanding of human subjects research, often supported by a relevant bachelor's or master's degree. Familiarity with electronic protocol management systems, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are highly valued. Strong attention to detail, analytical thinking, and effective communication skills set outstanding IRB Analysts apart. These qualities are crucial to ensure thorough, ethical review of research protocols and strict adherence to regulatory standards, protecting the rights and welfare of research participants.

What are some common challenges faced by IRB analysts in their daily work?

IRB Analysts frequently navigate complex regulatory requirements while reviewing a diverse range of research protocols, which can present challenges in interpreting guidelines and ensuring full compliance. They must balance efficiency with thoroughness, often working under tight deadlines to support both researchers and institutional standards. Staying current with evolving ethical standards and federal regulations is essential, as is effectively communicating decisions to investigators who may have varying levels of experience. Despite these challenges, the IRB Analyst role is rewarding for those who value ethical oversight and enjoy collaborative, detail-oriented work.

What do you need to be an IRB analyst?

To become an IRB analyst, candidates typically need a bachelor's degree in a related field such as healthcare, research, or ethics, along with experience in research compliance or regulatory environments. Knowledge of federal regulations like the Common Rule and Good Clinical Practice (GCP) is essential, and certifications such as the Certified IRB Professional (CIP) can enhance qualifications. Strong attention to detail, analytical skills, and the ability to review research protocols are also important for the role.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements set by Institutional Review Boards. They evaluate study procedures, consent forms, and risk assessments, often using specialized software, to protect research participants and maintain compliance. IRB analysts typically have a background in research ethics, healthcare, or related fields and work closely with researchers and regulatory bodies.

What are the most commonly searched types of Irb Analyst jobs in Minnesota?

The most popular types of Irb Analyst jobs in Minnesota are:

What are popular job titles related to Irb Analyst jobs in Minnesota?

For Irb Analyst jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Irb Analyst jobs?

Cities in Minnesota with the most Irb Analyst job openings:

Infographic showing various Irb Analyst job openings in Minnesota as of August 2026, with employment types broken down into 80% Full Time, 13% Part Time, and 7% Contract. Highlights an 66% In-person, 7% Hybrid, and 27% Remote job distribution, with an average salary of $71,753 per year, or $34.5 per hour.

Investigational Pharmacist

LCMC Health

Hibbing, MN • On-site

Full-time

Posted 3 days ago

New


LCMC Health rating

6.7

Company rating: 6.7 out of 10

Based on 128 frontline employees who took The Breakroom Quiz

534th of 893 rated healthcare providers


Job description

Your job is more than a job.

Responsible for implementing hospital and/or service line goals within the area. Performs other duties as assigned.

GENERAL DUTIES

  • Performing day-to-day dispensing and accountability activities with regard to IRB-approved clinical trials.
  • Establishing internal policies and procedures for developing and maintaining an Investigational Drug management system, which includes technical procedures for product ordering, adequate and safe receipt, handling, storage, dispensing, retrieval of unused product from subjects or researchers, and disposition of Investigational Medications (including documentation thereof).
  • Consulting with University Medical Center New Orleans Research Staff to support research during the planning phase of investigator-initiated and sponsored clinical trials research, including but not limited to: (a) serving as a resource to Research Staff for issues of protocol budgeting, pharmacy reimbursement and patient flow logistics; (b) serving as a resource to Research Staff for issues of pharmacy relations with sponsors; and (c) serving as a resource to the IRB.
  • Maintain a system for the inventory, distribution and dispensing of medications used in IRB-approved clinic trial research conducted under the auspices of University Medical Center New Orleans's IRB. This includes receiving, accountability, inventorying, and returning/destroying all medications furnished under an IRB-approved protocol.
  • For clinical trials where the PI controls the Investigational Drug at UMC, as approved by the IRB pursuant to a project-specific management plan, consult with the PI and Research Staff to ensure compliance with protocol and regulatory specifications for dispensing and, as requested by the IRB, to conduct audits of dispensing activity to the extent that such dispensing occurs through an IRB-approved management plan.
  • Integrate scheduling of research therapy into standard treatment regimens for IRB-approved clinical trials, as appropriate.
  • Maintain an archive of current and previous research protocols, manuals of procedures, and research informed consent and prescriptions for subjects at UMC.
  • Prepare protocol-mandated records and reports on drug utilization and inventory.
  • Participate in all site visits and audits at UMC as required by the FDA, OHRP, sponsors, regulatory or credentialing bodies.
  • Prepare industry- or government-supplied pharmaceuticals (including medications where a UMC employee holds the IND for the Drug being tested) for administration to subjects at UMC per a University Medical Center New Orleans IRB-approved protocol.
  • Obtain copies of adverse drug reactions documented and supplied by investigators or staff for subjects/patients receiving sponsor-supplied Investigational Drug or where a UMC employee holds the IND for the Drug being tested.
  • Ensures adequate staff coverage for assigned department areas according to projected patient load and established budget.
  • Monitors the day-to-day operations of assigned department staff, reacting effectively and efficiently to unplanned circumstances, demands and challenges facing the department to ensure consistent quality of service.
  • Demonstrates expertise in hospital and department processes and keeps staff updated by remaining current with hospital and department guidelines, federal, state, regulatory & other governing policies, procedures or guidelines.
  • Coordinates the departmental staff performance and improvement process, including the preparation, analysis and submission of required reports.
  • Updates and improves the department processes and workflows.
  • Participates as requested on teams, committees, and special projects, both internal and external, relating to investigation services.
  • Functions as a staff pharmacist as workload and personnel shortages require.

EXPERIENCE QUALIFICATIONS

Minimum of 3 year's post-graduate pharmacist experience in institutional pharmacy preferred; preferably 3 or more years of progressive responsibility. Experience in research-based activities preferred.

LICENSES AND CERTIFICATIONS

Louisiana licensed pharmacist or eligible.

WORK SHIFT:

Days (United States of America)

LCMC Health is a community.

Our people make health happen. While our NOLA roots run deep, our branches are the vessels that carry our mission of bringing the best possible care to every person and parish in Louisiana and beyond and put a little more heart and soul into healthcare along the way. Celebrating authenticity, originality, equity, inclusion and a little "come on in" attitude is the foundation of LCMC Health's culture of everyday extraordinary

About University Medical Center

University Medical Center, a world class academic medical center in LCMC Health's incredible community of care, is the largest medical training center for healthcare professionals in Louisiana and has long served as the region's safety net hospital for poor and underserved communities for 300+. Learn more about University Medical Center's legacy and our vision of becoming the epicenter of medical care, education, and research.

Your extras

  • Deliver healthcare with heart.
  • Give people a reason to smile.
  • Put a little love in your work.
  • Be honest and real, but with compassion.
  • Bring some lagniappe into everything you do.
  • Forget one-size-fits-all, think one-of-a-kind care.
  • See opportunities, not problems - it's all about perspective.
  • Cheerlead ideas, differences, and each other.
  • Love what makes you, you - because we do

You are welcome here.

LCMC Health is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

The above job summary is intended to describe the general nature and level of the work being performed by people assigned to this work. This is not an exhaustive list of all duties and responsibilities. LCMC Health reserves the right to amend and change responsibilities to meet organizational needs as necessary.

Simple things make the difference.

1. To get started, take your time to fully and accurately complete the application for employment. Incomplete applications get bogged down and are often eliminated due to missing information.

2. To ensure quality care and service, we may use information on your application to verify your previous employment and background.

3. To keep our career applications up-to-date, applications are inactive after 6 months and, therefore, require a new application for employment to be completed.

4. To expedite the hiring process, proof of citizenship or immigration status will be required to verify your lawful right to work in the United States.


What LCMC Health employees say

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About LCMC Health

Sourced by ZipRecruiter

LCMC Health, located in New Orleans, Louisiana, US, is a non-profit health system committed to providing high-quality healthcare services. Established in the year 2009, the company operates in the healthcare industry and dexterously manages several institutions, including children’s hospitals, academic medical centers, and local area hospitals. Employing over 8,500 skilled professionals across its network, LCMC Health's mission is to provide healthcare that goes beyond the ordinary to make a positive difference in every life it touches. Their core values encapsulate this mission too, prominently featuring care, innovation, trust, and respect.

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

New Orleans, LA, US

Year founded

2009

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