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Clinical Science Jobs in Indiana (NOW HIRING)

Lilly

Clinical Data Associate

Indianapolis, IN · On-site

The role is responsible for providing clinical data science leadership and ownership for a particular clinical study, set of studies, or programs. Primary Responsibilities: This is intended to ...

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Clinical Science information

See Indiana salary details

$25.8K

$113.8K

$221.7K

How much do clinical science jobs pay per year?

As of Jun 10, 2026, the average yearly pay for clinical science in Indiana is $113,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,838.00 and $170,144.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Scientist, and why are they important?

To thrive as a Clinical Scientist, you need a solid grounding in biological or biomedical sciences, often supported by an advanced degree such as an MSc or PhD, along with relevant clinical laboratory experience. Familiarity with laboratory information management systems (LIMS), specialized diagnostic equipment, and certifications like HCPC registration (in the UK) are typically required. Analytical thinking, attention to detail, and effective communication are crucial soft skills for interpreting results and collaborating with healthcare teams. These competencies ensure accurate diagnostics, patient safety, and the advancement of medical research and treatments.

What are some common challenges faced by professionals in Clinical Science roles, and how can they be addressed?

Professionals in Clinical Science often encounter challenges such as managing complex clinical trial protocols, ensuring regulatory compliance, and coordinating effectively with cross-functional teams. Navigating changing study requirements and tight timelines can also be demanding. To address these challenges, it's important to stay organized, maintain up-to-date knowledge of regulatory guidelines, and foster strong communication with colleagues in clinical operations, data management, and regulatory affairs. Leveraging project management tools and proactively seeking clarification on study objectives can also help Clinical Scientists succeed in their roles.

What is the difference between Clinical Science vs Clinical Research Coordinator?

AspectClinical ScienceClinical Research Coordinator
Required CredentialsBachelor's or higher in life sciences, certifications like CCRP or CCRA often preferredBachelor's degree in health sciences or related field, often with certification like CCRP
Work EnvironmentPharmaceutical companies, biotech firms, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry and academia for drug development and clinical trialsPrimarily in clinical trial sites managing patient data and study logistics

Clinical Science professionals focus on designing, analyzing, and overseeing clinical trials, often working in labs or industry settings. Clinical Research Coordinators manage day-to-day trial operations at research sites, ensuring protocol adherence and patient safety. Both roles require similar credentials but differ in responsibilities and work environments.

What is clinical science?

Clinical science is a field of study that focuses on research and practices related to human health and disease, particularly as they apply to patient care. It involves the investigation of the causes, development, diagnosis, and treatment of illnesses through laboratory research, clinical trials, and patient-focused studies. Professionals in clinical science often work in hospitals, research institutions, or pharmaceutical companies, contributing to advances in medical knowledge and healthcare. The field bridges the gap between laboratory research and clinical practice, ensuring that scientific discoveries lead to improved patient outcomes.
What are popular job titles related to Clinical Science jobs in Indiana? For Clinical Science jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Science jobs in Indiana look for? The top searched job categories for Clinical Science jobs in Indiana are:
What cities in Indiana are hiring for Clinical Science jobs? Cities in Indiana with the most Clinical Science job openings:
Clinical Science jobs near you
Infographic showing various Clinical Science job openings in Indiana as of June 2026, with employment types broken down into 3% As Needed, 71% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $113,754 per year, or $54.7 per hour.
Senior Scientist - Clinical Development, Animal Health

Senior Scientist - Clinical Development, Animal Health

Elanco Animal Health Incorporated

Greenfield, IN • On-site

Full-time

Retirement, PTO

Posted 6 days ago

Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

41st of 71 rated pharmaceutical

Job description

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!
Job Description
Position Description This is not a bench research, laboratory, or basic discovery role. This is a high-visibility, execution-focused Clinical Operations leadership role.
The Senior Scientist - Clinical Operations is fully responsible for the operational planning, vendor oversight, and hands-on execution of Target Animal Safety (TAS) and effectiveness studies. You will act as the primary Study Director or Sponsor Monitor, ensuring that trials conducted through external Contract Research Organizations (CROs) and field sites are delivered on time, within budget, and in strict compliance with regulatory standards. If your background is strictly in data analysis, lab work, or academic research without direct clinical trial project management and vendor oversight, this role is not aligned.
Key Responsibilities
  • Operational Study Ownership: Lead the operational end-to-end execution of TAS and effectiveness studies, moving trials seamlessly from concept protocol to final study report.
  • Vendor & CRO Management: Serve as the primary point of contact for CROs, university research sites, and private investigators. Manage site selection, study timelines, protocol deviations, and vendor accountability.
  • Protocol & Document Management: Author, review, and refine clinical study protocols, amendments, and data collection forms ensuring operational feasibility.
  • Compliance & Quality: Ensure all study activities rigidly adhere to FDA-CVM, VICH, GLP, and GCP guidelines. Monitor data integrity and troubleshoot field execution issues in real-time.
  • Cross-Functional Collaboration: Partner directly with Regulatory Affairs, Biostatistics, and Formulation R&D to translate scientific strategy into flawless operational execution.

Minimum Qualifications
  • Ph.D., DVM, or Master's/Bachelor's degree in Animal Science, Toxicology, Pharmacology, Physiology, or a related scientific/clinical discipline with equivalent years of direct trial management experience.
  • Experience: 5+ years of hands-on clinical trial operations or study management specifically within the Animal Health industry or a veterinary-focused CRO.
  • Study Expertise: Demonstrated experience managing Target Animal Safety (TAS) and/or pivotal target animal effectiveness studies.
  • Vendor Oversight: Proven track record of directly managing external partners, CROs, or clinical investigators.
  • Regulatory Knowledge: Robust, working knowledge of FDA-CVM regulations, GLP, and GCP requirements for veterinary species.

Preferred Qualifications
  • Direct experience acting as a Study Director or Sponsor Monitor for regulated target animal studies.
  • Experience across multiple veterinary species (companion animals and livestock/food animal species).
  • A proven background in troubleshooting clinical field trial logistics (e.g., shipping, site non-compliance, unexpected animal health events).
  • Experience authoring or contributing directly to technical sections for regulatory submissions (e.g., INAD/NADA files).

What You Will Gain
  • Full ownership of study execution in a focused animal health environment
  • Direct impact on safety and effective decisions tied to product development
  • High visibility across R&D, regulatory, and external partners
  • Opportunity to work on multi-species programs with real-world application
  • A role built for execution, not bench or discovery work

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 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.

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