1

Irb Manager Jobs in Indiana (NOW HIRING)

... management requirements. This includes working with IRB protocols, FDA and ISO compliance standards, and conducting risk assessments. The role supports the execution of established strategic ...

... GCP, IRB, and all applicable regulatory requirements. This position requires strong attention to ... Manage scheduling of participants, visit scheduling, reminders, and protocolrelated procedures.

next page

Showing results 1-20

Irb Manager information

See Indiana salary details

$55.7K

$74.8K

$94.7K

How much do irb manager jobs pay per year?

As of Jun 13, 2026, the average yearly pay for irb manager in Indiana is $74,784.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,400.00 and $77,600.00 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 in the Irb Manager position, and why are they important?

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.

What is an IRB Manager job?

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 Indiana? The most popular types of Irb jobs in Indiana are:
What are popular job titles related to Irb Manager jobs in Indiana? For Irb Manager jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Irb Manager jobs? Cities in Indiana with the most Irb Manager job openings:
Infographic showing various Irb Manager job openings in Indiana as of June 2026, with employment types broken down into 16% Full Time, 81% Part Time, 2% Contract, and 1% Nights. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $74,784 per year, or $36 per hour.

Advanced Clinical Biomechanics Specialist

Imh

On-site

Full-time

Posted 4 days ago


Job description

Job Description:

Job Profile Summary
Advanced Medical Biomechanics Specialist role supports the advanced care technology and visualization engineering department, an enterprise-wide team dedicated to enhancing Intermountain's mission and vision. This position focuses on implementing advanced biomedical and visualization technologies and services, demonstrating clinical and business impact from research to practice, and transforming healthcare at Intermountain. The primary responsibilities include supporting the engineering execution and service delivery of advanced technology, biomedical and visualization service lines.
This role is crucial in Intermountain Healthcare's efforts to leverage technology to improve efficiencies and outcomes in clinical settings. The specialist will handle various engineering tasks related to advanced care technology and visualization engineering, continuous improvement of existing service lines, and the execution of new service lines, including implementation and validation.
Key requirements for this position include a deep understanding of human anatomy, radiologic anatomic analysis, medical modeling, 3D visualization, and 3D printing. The role also demands specialized knowledge and experience in clinical and surgical procedures that necessitate advanced visualization modalities. Additionally, the specialist must align tasks with a medical quality management system and have experience with healthcare and medical device regulatory, privacy, and risk management requirements. This includes working with IRB protocols, FDA and ISO compliance standards, and conducting risk assessments.
The role supports the execution of established strategic priorities in specific specialties, evaluating and implementing new advanced visualization technologies and solutions. The specialist will work closely with the department director and other stakeholders, with responsibilities growing as the department matures.

*Candidates with Radiologic Technician AART certifications or CFD & Fluid Mechanics Experience are encouraged to apply.


Essential Functions

  • Responsible for a wide variety of technical responsibilities as it relates to the advanced care technology and immersive visualization services execution and continuous improvement of already defined service lines and initiatives and direct the use of 3D printing for prototyping and demo product visualization.
  • Design, create, produce, engineer, Postprocess, and deliver services provided by the Advanced Visualization engineering team as needed.
  • Execution of newly formed service lines, including implementation and validation of new design concepts to meet the needs of the relevant stakeholders.
  • Apply knowledge of medical device design and 3D visualization (XR and Spatial Computing) and 3D printing technologies and associated postprocessing techniques and tools, in delivering the Advanced Visualization services
  • Implement quality assurance standards such as ISO 13485, including relevant techniques
  • Maintain equipment according to timelines and schedules to ensure accurate and repeatable 3D design, prototype, and model production.
  • Align tasks and work done to a given medical quality management system leveraging previous experienced in healthcare and medical device regulatory, privacy, and risk management requirements.
  • Execute of established strategic priorities in evaluating and implementing new advanced visualization technologies and solutions.
  • Execute the day-to-day engineering needs for the department
  • Recommends and implements solutions, including support.
  • Prepares and ensures accuracy of documentation of services and operations.

Skills

  • Patient-specific biomedical technology development
  • Visceral anatomy segmentation and quantitative assessment
  • Complex anatomy Reconstruction
  • Patient specific Medical Device Design
  • CFD and Fluid Mechanics Experience

Radiologic Technicians with AART certifications are encouraged to apply

Qualifications

  • Bachelor's degree in mechanical engineering, biomechanical, biomedical or closely related discipline.
  • Post-graduation experience of hands-on verifiable specific experience performing anatomic medical modeling, surgical guides design, diagnostic imaging processing, and 3D printing, and medical device development experience in an advanced visualization program.
  • Two years' experience must be spent performing high volume of the needed specialty with aforementioned relevant experience, certain specialty might be required at the time.


PLUS (in addition to education and experience above) Demonstrated tangible performance of ALL the following is required:

  • Design/case Portfolio is required.
  • Medical regulatory and Quality (i.e. ISO, 510k, etc..).
  • Demonstrated hands-on experience with patient specific 3D printed modeling and surgical guides design
  • Experience with medical device design.
  • Demonstrated medical device regulator and quality management system experience
  • Demonstrated hands-on experience with Mixed reality, 3D printing and product prototyping, and POC.
  • Proficient in one or more of the proprietary 3D design and anatomic modeling software programs.
  • Proficient with reconstruction of soft tissue/visceral/cardiology/neuro/etc. in various specialties including counts of cases and experience portfolio.
  • Skilled and experienced in maintenance and oversight of multiple 3D printing technologies, with minimum polyjet, SLS, and SLA printers.
  • Demonstrated self-motivation skills and ability to independently apply analytical skills and scientific technical principles in problem solving and development.
  • Demonstrated experience with academic literature review, grant funding, research design, and analysis.
  • Demonstrated ability to work with many stakeholders, curate ideas and input and deliver, and validate customer needs.

Preferred:

  • Masters of Science degree in Mechanical or biomechanical engineering with to 3 years of relevant aforementioned verifiable experience.
  • ISO13458 experience and certification.
  • 510k submission experience.
  • Python Programing Experience
  • Quality Assurance and Risk Analysis.
  • Medical Device design experience.
  • Experience with a wide variety of additive manufacturing, e.g. Stratasys FDM Thermoplastics and PolyJet Photopolymers 3D printers and knowledge of subtractive manufacturing, e.g. AWJ
  • Experience with a molding and related manufacturing and prototyping techniques.
  • Experience with Microsoft Project or equivalent project planning software
  • Strong understanding of intellectual property (IP) considerations
  • The ability to effectively prioritize and execute tasks in a high-pressure environment is crucial.
  • Proven analytical and problem-solving abilities with strong written and oral communication skills.
  • Highly self-motivated and directed with high level of attention to detail.


Physical Requirements

  • Operate equipment, tools, and computers requiring the ability to move fingers and hands.
  • See and read computer monitors and documents.
  • This role will on occasion require outside of regular hours and weekend support
  • Lifting, operating, and maintaining lab
*Depending on skillset & years of experience, there is potential for this role to be filled at the senior level. $39.57 - $62.29 USD Hourly.
*This position is eligible for relocation assistance.

Location:

Vine Street Office Building

Work City:

Murray

Work State:

Utah

Scheduled Weekly Hours:

40

The hourly range for this position is listed below. Actual hourly rate dependent upon experience.

$32.10 - $50.57

We care about your well-being - mind, body, and spirit - which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.

Learn more about our comprehensive benefits package here.

Intermountain Health is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

At Intermountain Health, we usethe artificial intelligence ("AI") platform, HiredScore to improve your job application experience.HiredScore helps match your skills and experiences to the best jobs for you. WhileHiredScore assists in reviewing applications, all final decisions are made byIntermountain personnel to ensure fairness. We protect your privacy and follow strict data protection rules. Your information is safe and used only for recruitment. Thank you for considering a career with us and experiencing our AI-enhanced recruitment process.

All positions subject to close without notice.