Clinical Research Associate Jobs in Indiana
Clinical Research Associate jobs in Indiana are concentrated in Indianapolis, Bloomington, and South Bend, where major research institutions and pharmaceutical companies maintain deep hiring pipelines at every level from entry-level coordinator to senior CRA. Eli Lilly and Company, Indiana University Health, and Covance are among the most established employers in the state, with consistent demand for clinical research associates in oncology, cardiovascular trials, and Phase II through Phase IV studies. Indiana's life sciences sector keeps this one of the more active Midwest markets for the role. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 26+ Clinical Research Associate 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 a Clinical Research Associate (CRA) – Animal Health, you will be a key member of the global Research & Development organization, supporting the execution of clinical studies for our innovative Farm Animal and Pet Health products. You will be responsible for ensuring studies are conducted to the highest standards, that data is captured accurately, and that we maintain compliance with all global regulatory guidelines. This role is critical to advancing Elanco’s pipeline and bringing new solutions to our customers.
Your Responsibilities:
- Perform and manage all clinical monitoring activities, including site qualification, initiation, routine monitoring, and close-out visits to ensure studies adhere to protocol, GCP/VICH guidelines, and Elanco standards.
- Serve as the primary point of contact for clinical trial sites (CROs and internal), building strong relationships and providing oversight to ensure study success and data integrity.
- Conduct thorough data review and source data verification, working with site personnel to resolve data queries promptly and ensure the accuracy and completeness of all study documentation.
- Proactively identify and mitigate site-level risks, monitor for and report protocol deviations or safety events (AEs/SAEs), and support internal QA reviews or regulatory inspections.
- Collaborate closely with cross-functional partners (Clinical Development, Data Management, Biostatistics, Regulatory Affairs, QA) to ensure seamless project delivery and support the development of regulatory submission files.
What You Need to Succeed (minimum qualifications):
- Education: Bachelor's Degree in a life science or health-related field or High School Diploma with 8 years of experience.
- Experience: A minimum of 2 years of experience in clinical research, with specific experience in a monitoring or site management role.
- Top 2 skills: Demonstrated proficiency with clinical trial processes (GCP/VICH), data management systems (EDC), and collaborative tools (e.g., Veeva, MS Office). Strong communication and interpersonal skills with the ability to work effectively across interdisciplinary teams.
What will give you a competitive edge (preferred qualifications):
- Master's degree in a relevant scientific field.
- Experience in the animal health industry.
- Professional certification (e.g., CCRA, CCRC).
- Experience with both farm animal and companion animal studies.
Additional Information:
- Travel: Up to 50% (US and International).
- 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 a Clinical Research Associate (CRA) – Animal Health, you will be a key member of the global Research & Development organization, supporting the execution of clinical studies for our innovative Farm Animal and Pet Health products. You will be responsible for ensuring studies are conducted to the highest standards, that data is captured accurately, and that we maintain compliance with all global regulatory guidelines. This role is critical to advancing Elanco’s pipeline and bringing new solutions to our customers.
Your Responsibilities:
- Perform and manage all clinical monitoring activities, including site qualification, initiation, routine monitoring, and close-out visits to ensure studies adhere to protocol, GCP/VICH guidelines, and Elanco standards.
- Serve as the primary point of contact for clinical trial sites (CROs and internal), building strong relationships and providing oversight to ensure study success and data integrity.
- Conduct thorough data review and source data verification, working with site personnel to resolve data queries promptly and ensure the accuracy and completeness of all study documentation.
- Proactively identify and mitigate site-level risks, monitor for and report protocol deviations or safety events (AEs/SAEs), and support internal QA reviews or regulatory inspections.
- Collaborate closely with cross-functional partners (Clinical Development, Data Management, Biostatistics, Regulatory Affairs, QA) to ensure seamless project delivery and support the development of regulatory submission files.
What You Need to Succeed (minimum qualifications):
- Education: Bachelor's Degree in a life science or health-related field or High School Diploma with 8 years of experience.
- Experience: A minimum of 2 years of experience in clinical research, with specific experience in a monitoring or site management role.
- Top 2 skills: Demonstrated proficiency with clinical trial processes (GCP/VICH), data management systems (EDC), and collaborative tools (e.g., Veeva, MS Office). Strong communication and interpersonal skills with the ability to work effectively across interdisciplinary teams.
What will give you a competitive edge (preferred qualifications):
- Master's degree in a relevant scientific field.
- Experience in the animal health industry.
- Professional certification (e.g., CCRA, CCRC).
- Experience with both farm animal and companion animal studies.
Additional Information:
- Travel: Up to 50% (US and International).
- 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 26 Clinical Research Associate Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
Find JobsClinical Research Associate Jobs by City in Indiana
Where Indiana roles are concentrated, by current openings.
Clinical Research Associate 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 associate jobs across Indiana.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Society of Clinical Research Associates or ACRP certification preferred or required
- Minimum two years of clinical trial monitoring or coordination experience expected
- Proficiency with electronic data capture systems such as Medidata Rave or Veeva Vault
- Knowledge of ICH-GCP guidelines and FDA regulations governing clinical research
- Willingness to travel to investigative sites across Indiana and occasionally out of state
Clinical Research Associate Jobs in Indiana: Frequently Asked Questions
How do you become a clinical research associate in Indiana?
Start with a bachelor's degree in a life science, nursing, or a health-related field, which is the baseline most Indiana employers require. Indiana does not issue a state license specific to clinical research associates, so professional certification carries the most weight: the Certified Clinical Research Associate credential from the Society of Clinical Research Associates or the CCRA from ACRP are the most widely recognized. Many candidates enter through clinical trial coordinator roles at Indiana University Health or Eli Lilly before moving into monitoring.
Which companies hire clinical research associates in Indiana?
Indiana clinical research associate roles are posted by Indiana University, Elanco, and Eli Lilly and others right now, based on current listings on Migrate Mate as of November 2026. Indiana's strong pharmaceutical and academic medical presence, anchored by Eli Lilly's global headquarters in Indianapolis, means the state sustains consistent CRA demand year-round.
Which Indiana cities have the most clinical research associate jobs?
Indianapolis, Indiana, and Hobart account for the largest share of clinical research associate openings in Indiana. Indianapolis drives the majority of postings because Eli Lilly's headquarters, Indiana University School of Medicine, and a cluster of contract research organizations are all based there, while Bloomington and South Bend draw openings from IU Health and Beacon Health System respectively.
Are there remote clinical research associate jobs in Indiana?
Yes, and more than many clinical roles, because a significant portion of CRA work involves reviewing data, writing monitoring reports, and communicating with sponsors rather than hands-on patient care. About 75% of clinical research associate openings tied to Indiana are remote or hybrid as of November 2026, though site visit requirements vary by sponsor. Fully remote positions tend to be concentrated in post-monitoring report review and central monitoring functions.
How can I get hired as a clinical research associate in Indiana with little or no experience?
The most realistic entry path is a clinical research coordinator role, which Indiana University Health and several Indianapolis-area contract research organizations regularly hire for at the junior level without prior monitoring experience. From there, coordinators build the site-side knowledge CRA managers value most. Pursuing the ACRP Certified Clinical Research Coordinator credential while coordinating signals readiness to move into monitoring. Candidates with a nursing or pharmacy background often transition directly into associate CRA positions at Covance or Fortrea's Indiana sites.
Where can I find and apply to clinical research associate jobs in Indiana?
You can find and apply to clinical research associate jobs in Indiana on Migrate Mate, which lists current Indiana openings. Search the available roles, identify the ones that match your experience and preferred location, and apply directly to the ones that fit.
See All 26 Clinical Research Associate Jobs in Indiana
Find roles in Indiana that match your experience and apply in just a few clicks.
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