Clinical Research Jobs in Indiana
Clinical Research jobs in Indiana are concentrated in Indianapolis, Bloomington, and West Lafayette, where major employers like Eli Lilly and Company, Indiana University Health, and Purdue University drive consistent demand for coordinators, associates, and principal investigators. The most in-demand specialties are oncology trials, Phase II-IV pharmaceutical studies, and regulatory affairs, reflecting Indiana's deep pharmaceutical manufacturing base. Openings range from entry-level research coordinator roles to senior clinical operations positions. See the openings below and apply to the ones that match your experience.
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Showing 5 of 28+ Clinical Research 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 Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Indiana
Where Indiana roles are concentrated, by current openings.
Clinical Research 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 jobs across Indiana.
- SOCRA or ACRP certification (CCRP or CCRC) recognized by Indiana employers
- Bachelor's degree in life sciences, nursing, pharmacy, or a related health field
- Experience with FDA regulations, GCP guidelines, and IRB submission processes
- Proficiency in electronic data capture systems such as Medidata Rave or Oracle InForm
- Strong understanding of informed consent procedures and protocol deviation reporting
- Ability to coordinate multiple concurrent trials and communicate with multi-site teams
Clinical Research Jobs in Indiana: Frequently Asked Questions
How do you become a clinical research in Indiana?
Most Indiana employers hire candidates with a bachelor's degree in a life science, nursing, or health-related field, followed by on-the-job training under a supervising investigator or coordinator. Indiana does not issue a state license specific to clinical research, but employers widely expect candidates to hold or pursue SOCRA's CCRP or ACRP's CCRC certification, both of which require documented trial experience and a passing exam score. Starting as a research assistant or data coordinator at a hospital system or pharmaceutical company is the most common entry path.
Which companies hire clinical researchs in Indiana?
Indiana clinical research 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 pharmaceutical corridor, anchored by Eli Lilly's Indianapolis headquarters and a network of contract research organizations across the state, generates particularly steady demand for coordinator and regulatory roles.
Which Indiana cities have the most clinical research jobs?
Indianapolis, Munster, and Indiana account for the largest share of clinical research openings in Indiana. Indianapolis leads because it is home to Eli Lilly's global headquarters, Indiana University Health's research network, and multiple contract research organizations, while Bloomington and West Lafayette benefit from Indiana University and Purdue University's active clinical and translational research programs, which anchor hiring in those smaller metros.
Are there remote clinical research jobs in Indiana?
Yes, but they're less common than in purely desk-based fields, since many clinical research tasks such as patient visits, specimen handling, and on-site monitoring require physical presence. About 75% of clinical research openings tied to Indiana are remote or hybrid as of October 2026, reflecting selective flexibility in the field. Roles most likely to allow remote work include regulatory affairs coordinators, data managers, and study start-up specialists whose responsibilities are document- and system-driven rather than site-based.
How can I get hired as a clinical research in Indiana with little or no experience?
The most realistic entry path is applying for a research coordinator I or clinical research assistant position at an Indiana academic medical center or large hospital system, where structured onboarding and mentorship are built into the role. Indiana University Health and Eskenazi Health in Indianapolis, along with Purdue's clinical research units in West Lafayette, regularly bring on candidates who hold a relevant bachelor's degree but lack direct trial experience. Completing a Good Clinical Practice training course and earning an IATA certification for biological specimen shipping can meaningfully strengthen an entry-level application, as can any adjacent experience in patient care, data entry, or regulatory documentation.
Where can I find and apply to clinical research jobs in Indiana?
You can find and apply to clinical research jobs in Indiana on Migrate Mate, which lists current openings from employers across the state. Search the listings to find roles that match your experience level and specialty, then apply directly to the ones that fit. No sign-up is required to view the openings.
See All 28 Clinical Research Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find Clinical Research Jobs