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Institutional Review Board Jobs in Indiana (NOW HIRING)

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Pharmacy Drug Info Specialist

Indianapolis, IN · On-site

$19.50 - $25.25/hr

Actively participate as a member of the Institutional Review Board. * Engage in various aspects of the pharmacy residency program, including serving as a preceptor in Drug Information. * Additional ...

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Institutional Review Board information

See Indiana salary details

$48.5K

$79.7K

$127K

How much do institutional review board jobs pay per year?

As of Sep 8, 2026, the average yearly pay for institutional review board in Indiana is $79,657.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,700.00 and $93,700.00 per year, depending on experience, location, and employer.

What does an institutional review board professional do?

An IRB professional is responsible for reviewing research studies involving human subjects to ensure they meet ethical and regulatory standards. They assess protocols for compliance with federal, state, and institutional guidelines to protect participant rights and welfare. Their duties include reviewing applications, providing guidance to researchers, and ensuring informed consent processes are properly implemented. IRB professionals often work in universities, hospitals, or research institutions.

What are the key skills and qualifications needed to thrive in an institutional review board position?

To thrive as an Institutional Review Board (IRB) member or administrator, you need a strong understanding of research ethics, federal regulations, and compliance requirements, often supported by a background in health sciences, law, or ethics. Familiarity with electronic IRB management systems, regulatory databases, and training in human subjects research protection (such as CITI certification) is typically required. Attention to detail, critical thinking, and the ability to communicate diplomatically with diverse stakeholders are crucial soft skills. These abilities are essential to ensure the ethical review and approval of research projects, safeguarding participants and maintaining institutional integrity.

What are some typical challenges faced by professionals working on an institutional review board?

Professionals working on an Institutional Review Board often navigate the complex balance between facilitating innovative research and upholding strict ethical standards to protect human subjects. One common challenge is keeping current with frequently evolving regulations and interpreting how they apply to a wide range of research proposals. IRB members must also manage high volumes of submissions and coordinate with researchers, legal advisors, and compliance officers to resolve issues promptly. This role requires continuous professional development and a collaborative approach to problem-solving in a multidisciplinary setting.

How to become an institutional review board reviewer?

To become an institutional review board (IRB) reviewer, individuals typically need relevant experience in research ethics, healthcare, or scientific fields, along with familiarity with federal regulations such as the Common Rule. Many IRB members have advanced degrees and may complete training programs on human subjects research protections. Active participation often requires being part of an institution that has an IRB and attending regular meetings to review research protocols.

How to get an Institutional Review Board job?

To work as an Institutional Review Board (IRB) member or staff, candidates typically need a background in research, ethics, or healthcare, along with knowledge of federal regulations such as the Common Rule. Relevant experience, professional certifications, and understanding of human subjects protection are often required, and positions may require a bachelor's or advanced degree. Training on IRB procedures and compliance is also beneficial for securing such roles.

What are the most commonly searched types of Institutional Review Board jobs in Indiana?

The most popular types of Institutional Review Board jobs in Indiana are:

What are popular job titles related to Institutional Review Board jobs in Indiana?

For Institutional Review Board jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Institutional Review Board jobs in Indiana look for?

The top searched job categories for Institutional Review Board jobs in Indiana are:

Institutional Review Board jobs near you
Infographic showing various Institutional Review Board job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 2% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $79,657 per year, or $38.3 per hour.

Research Nurse Coordinator

Innovative Hematology

Indianapolis, IN • On-site

Other

Re-posted 9 days ago

Job description

Research Nurse Coordinator

At Innovative Hematology, Inc. (IHI), we offer a future where people with rare blood disorders flourish. Our experts provide the highest quality comprehensive services and holistic care to patients with bleeding, clotting and other hematologic disorders, and to their families.

As a Research Nurse Coordinator, you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.

The opportunity includes:

  • Participate in the planning and execution of research projects under the direction of the Medical Director and the primary investigator.
  • Function as an integral part of the research and comprehensive care teams, working with colleagues to meet deadlines and maintain a flexible schedule based on the needs of patients, the department, and IHI.
  • Create a study budget in InfoED in collaboration with the finance department. Work with the finance department to assist with billing, invoicing, tracking status on payments due or past due, documenting patient stipend requests, and charting completed study visits.
  • Assess patients for inclusion and exclusion criteria to determine study eligibility, and work cooperatively with the comprehensive team to coordinate study-related patient care. Explain informed consent for each study participant; document refusals according to protocol.
  • Ensure accurate and prompt communication with patients, the primary investigator, research manager, external contacts, study sponsors, and monitors.
  • Prepare study-related documentation such as protocol worksheets, procedural manuals, drug dispensation records, regulatory forms, adverse event reports; submit all relevant study documents to the institutional review board.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices. Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • Participate in internal quality assurance; review monitor reports for trends across studies.

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