Clinical Research Nurse Jobs in Indiana
Clinical Research Nurse jobs in Indiana are concentrated in Indianapolis, Indianapolis suburbs like Carmel and Fishers, and the South Bend and Fort Wayne metros, where large academic medical centers and pharmaceutical-aligned health systems drive consistent hiring. Major employers with a lasting presence in Indiana include Indiana University Health, Eli Lilly and Company's clinical operations division, and Eskenazi Health, all of which run ongoing clinical trial programs. Oncology, cardiovascular, and neurology trials see the strongest demand for qualified research nurses across the state. See the openings below and apply to the ones that match your experience.
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Showing 5 of 28+ Clinical Research Nurse jobs
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
As the Senior Research Scientist – Farm Animal Clinical Development, Vaccines and Infectious Diseases, you will play a pivotal role in advancing Elanco’s farm animal innovation pipeline by designing, coordinating, and executing global host animal safety and efficacy study programs. In this role, you will formulate clinical development plans from inception through approval to deliver next-generation vaccines and therapeutic products to our customers. You will partner closely with cross-functional R&D teams, Regulatory Affairs, and external research partners to translate scientific strategy into high-impact regulatory submissions.
Your Responsibilities:
- Design, author, and execute robust host animal safety and efficacy study protocols and comprehensive clinical development plans in compliance with USDA, GLP, vGCP, and VICH standards.
- Partner with Clinical Development Sciences (CDS) to evaluate, select, and monitor qualified external research facilities, investigators, and contract research organizations (CROs).
- Collaborate cross-functionally with Biostatistics, Regulatory Affairs, Medical Writing, and Quality Assurance to analyze, interpret, and report clinical trial data for global regulatory submissions.
- Serve as a clinical and technical subject matter expert during regulatory agency interactions and scientific conferences, effectively communicating study data and strategy.
- Drive continuous improvement and technical excellence by updating functional procedures, mentoring less experienced colleagues, and staying current with advances in veterinary vaccines and infectious diseases.
What You Need to Succeed (minimum qualifications):
- Education: Master’s Degree in Animal Science, Veterinary Sciences, Microbiology, Immunology, or related scientific discipline (or Bachelor's Degree with equivalent level of relevant industry experience); DVM or Ph.D. warmly welcomed.
- Required Experience: A minimum of 3 years of experience in veterinary clinical study design, animal health research, or vaccine/biologics product development.
- Key Skills: Proven proficiency in designing host animal safety/efficacy protocols under GxP/VICH-GCP guidelines, combined with strong project organization and cross-functional communication abilities.
What will give you a competitive edge (preferred qualifications):
- DVM and/or Ph.D. in Veterinary Medicine, Animal Science, Immunology, Virology, or Infectious Diseases.
- 5+ years of direct experience leading farm animal vaccine or therapeutic clinical development programs.
- Demonstrated experience interacting with regulatory agencies (e.g., USDA-CVB, FDA-CVM, EMA) and authoring regulatory dossier sections.
- Hands-on expertise evaluating, selecting, and overseeing external contract research organizations (CROs) and university research facilities.
- Strong strategic mindset with demonstrated ability to translate complex scientific data into regulatory and commercial solutions.
Additional Information:
- Travel: 10–20% (Domestic and occasional International travel)
- Location: Global Elanco Headquarters - Indianapolis, IN - Hybrid Work Environment
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
#LI-MW1
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
As the Senior Research Scientist – Farm Animal Clinical Development, Vaccines and Infectious Diseases, you will play a pivotal role in advancing Elanco’s farm animal innovation pipeline by designing, coordinating, and executing global host animal safety and efficacy study programs. In this role, you will formulate clinical development plans from inception through approval to deliver next-generation vaccines and therapeutic products to our customers. You will partner closely with cross-functional R&D teams, Regulatory Affairs, and external research partners to translate scientific strategy into high-impact regulatory submissions.
Your Responsibilities:
- Design, author, and execute robust host animal safety and efficacy study protocols and comprehensive clinical development plans in compliance with USDA, GLP, vGCP, and VICH standards.
- Partner with Clinical Development Sciences (CDS) to evaluate, select, and monitor qualified external research facilities, investigators, and contract research organizations (CROs).
- Collaborate cross-functionally with Biostatistics, Regulatory Affairs, Medical Writing, and Quality Assurance to analyze, interpret, and report clinical trial data for global regulatory submissions.
- Serve as a clinical and technical subject matter expert during regulatory agency interactions and scientific conferences, effectively communicating study data and strategy.
- Drive continuous improvement and technical excellence by updating functional procedures, mentoring less experienced colleagues, and staying current with advances in veterinary vaccines and infectious diseases.
What You Need to Succeed (minimum qualifications):
- Education: Master’s Degree in Animal Science, Veterinary Sciences, Microbiology, Immunology, or related scientific discipline (or Bachelor's Degree with equivalent level of relevant industry experience); DVM or Ph.D. warmly welcomed.
- Required Experience: A minimum of 3 years of experience in veterinary clinical study design, animal health research, or vaccine/biologics product development.
- Key Skills: Proven proficiency in designing host animal safety/efficacy protocols under GxP/VICH-GCP guidelines, combined with strong project organization and cross-functional communication abilities.
What will give you a competitive edge (preferred qualifications):
- DVM and/or Ph.D. in Veterinary Medicine, Animal Science, Immunology, Virology, or Infectious Diseases.
- 5+ years of direct experience leading farm animal vaccine or therapeutic clinical development programs.
- Demonstrated experience interacting with regulatory agencies (e.g., USDA-CVB, FDA-CVM, EMA) and authoring regulatory dossier sections.
- Hands-on expertise evaluating, selecting, and overseeing external contract research organizations (CROs) and university research facilities.
- Strong strategic mindset with demonstrated ability to translate complex scientific data into regulatory and commercial solutions.
Additional Information:
- Travel: 10–20% (Domestic and occasional International travel)
- Location: Global Elanco Headquarters - Indianapolis, IN - Hybrid Work Environment
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
#LI-MW1
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
See All 28 Clinical Research Nurse Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find Clinical Research Nurse JobsClinical Research Nurse Jobs by City in Indiana
Where Indiana roles are concentrated, by current openings.
Clinical Research Nurse Job Market in Indiana
A snapshot from current Indiana openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
What Indiana Employers Look For
The qualifications that appear most often in clinical research nurse jobs across Indiana.
- Active registered nurse license issued or recognized by the Indiana Professional Licensing Agency
- Minimum two years of clinical nursing experience in a relevant specialty area
- Experience with clinical trial protocols, GCP guidelines, and regulatory documentation
- Certified Clinical Research Professional or Certified Clinical Research Coordinator credential preferred
- Proficiency with electronic data capture systems and clinical trial management software
- Strong patient assessment skills and ability to administer investigational treatments per protocol
Clinical Research Nurse Jobs in Indiana: Frequently Asked Questions
How do you become a clinical research nurse in Indiana?
You need an active registered nurse license issued by the Indiana Professional Licensing Agency, which requires passing the NCLEX-RN exam after completing an accredited nursing program. Most Indiana employers then look for at least one to two years of direct clinical experience before hiring into a research role. From there, earning a credential such as the Certified Clinical Research Professional through the Society of Clinical Research Associates strengthens your application considerably and is increasingly expected at Indiana academic medical centers.
Which companies hire clinical research nurses in Indiana?
Indiana clinical research nurse roles are posted by Eli Lilly, Indiana University, and Profound Research and others right now, based on current listings on Migrate Mate as of October 2026. Indiana's deep pharmaceutical industry roots, anchored by Eli Lilly's Indianapolis headquarters, make it one of the more active states for industry-sponsored trial nursing roles alongside academic medical center positions.
Which Indiana cities have the most clinical research nurse jobs?
Indianapolis, Munster, and Indiana have the most clinical research nurse openings in Indiana. Indianapolis dominates the distribution because it is home to IU Health's research network, Eskenazi Health, and Eli Lilly's clinical operations, while South Bend and Fort Wayne openings are largely tied to Beacon Health System and Parkview Health, both of which run active trial programs in their respective regions.
Are there remote clinical research nurse jobs in Indiana?
Yes, but they're rare. About 75% of clinical research nurse openings tied to Indiana are remote or hybrid as of October 2026, reflecting that most trial nursing duties require direct patient contact, specimen collection, and on-site protocol administration. The portions of the role most likely to go remote are regulatory documentation, participant follow-up calls, and data entry tasks, which some Indiana employers allow from home on a part-time basis.
How can I get hired as a clinical research nurse in Indiana with little or no experience?
The most realistic entry path is applying to research coordinator or clinical research associate roles at Indiana academic medical centers such as IU Health or Eskenazi Health, both of which periodically hire nurses transitioning from bedside care into research support positions. Nurses moving from oncology, cardiology, or infusion units carry directly transferable skills and are frequently considered. Completing a Good Clinical Practice certification before applying and volunteering on a departmental trial at your current employer are the two steps that most consistently help Indiana candidates without formal research experience clear the initial screening.
Where can I find and apply to clinical research nurse jobs in Indiana?
You can find and apply to clinical research nurse jobs in Indiana on Migrate Mate, which lists current Indiana openings. Search the listings, find the roles that fit your background and location, and apply directly to the ones that match.
See All 28 Clinical Research Nurse Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find Clinical Research Nurse Jobs