Research Scientist - Product development

Indiana Ag Connection; Indianapolis (IN); Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Relocation packages

Two weeklong shutdowns (mid-summer and

8-week parental leave

Employee Resource Groups

Annual bonus offering

Flexible work arrangements

401K matching

Job summary

Elanco in Indianapolis, IN, is seeking a Clinical Development Scientist - Parasiticides to lead global clinical programs for farm and companion animal parasiticides from early development through regulatory submission.

You will design study protocols, coordinate cross-functional teams, and ensure GLP/vGCP compliance to deliver high-quality data for regulatory authorities. A hybrid work arrangement and travel up to 20% are expected.

Qualifications

• Education: DVM or PhD in Animal Science or related field preferred; MS with relevant experience will be considered.
• Top Skills: Strong project management and organizational capabilities, excellent written and verbal communication skills.

Responsibilities

• Lead the planning and execution of global clinical programs, including pilot and pivotal studies, ensuring compliance with GLP, vGCP, VICH, and other applicable regulatory standards.
• Develop comprehensive clinical development plans, author study protocols and reports, and collaborate with cross-functional partners to deliver programs on time and with high-quality standards.
• Design and oversee efficacy and TAS studies in partnership with Clinical Development Sciences, Biostatistics, Regulatory Affairs, and external research facilities to support global regulatory approvals.
• Analyze and interpret study data with support from Data Management, Medical Writing, and internal/external reviewers; prepare documentation and support submissions and presentations to regulatory authorities and scientific forums.
• Ensure quality assurance and regulatory compliance while contributing to process improvements, procedural development, and continuous advancement of clinical development practices.

Skills

Project management

Communication skills

Education

DVM or PhD in Animal Science or related field

MS with relevant experience

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!

Your Role: Clinical Development Scientist - Parasiticides

As a Clinical Development Scientist, you will lead the development and execution of global companion and farm animal parasiticide clinical programs supporting Elanco's innovation pipeline. In this role, you will design, coordinate, and deliver high-quality clinical effectiveness and target animal safety (TAS) studies from early development through regulatory approval in initial targetgeographies.

Your Responsibilities:

• Lead the planning and execution of global clinical programs, including pilot and pivotal studies, ensuring compliance with GLP, vGCP, VICH, and other applicableregulatory standards.
• Develop comprehensive clinical development plans, author study protocols and reports, and collaborate with cross-functional partners to deliver programs on time and with high-quality standards.
• Design and oversee efficacy and TAS studies in partnership with Clinical Development Sciences, Biostatistics, Regulatory Affairs, and external research facilities to support global regulatory approvals.
• Analyze and interpret study data with support from Data Management, Medical Writing, and internal/external reviewers; prepare documentation and support submissions and presentations to regulatory authorities and scientific forums.
• Ensure quality assurance and regulatory compliance while contributing to process improvements, procedural development, and continuous advancement of clinical development practices.

What You Need to Succeed (minimum qualifications):

• Education: DVM or Ph.D. in Animal Science or related field preferred; MS with relevant experience will be considered. Advanced degree in addition to DVM is desirable.
• Top Skills: Strong project management and organizational capabilities, excellent written and verbal communication skills.

What Will Give You a Competitive Edge (preferred qualifications):

• Proven experience interacting with regulatory authorities and supporting product registrations.
• Working knowledge of GCP, GLP, GMP, and global regulatory frameworks.
• Demonstrated ability to lead and influence cross-functional teams and external research partners.
• Strategic mindset with the ability to drive clinical programs and align stakeholders.
• Understanding of research and development processes within animal health or pharmaceutical industries.

Additional Information:

• Travel: 10-20% domestic, with potential international travel.
• Location: 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 highlightsinclude:

• 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.