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Clinical Development Scientist Jobs (NOW HIRING)

The Development Scientist I will serve as the primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Development ...

The Development Scientist II is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. Position ...

... toward clinical trials. Key Responsibilities: * Design, conduct and optimize R&D studies to ... Stay current with advancements in radiopharmaceutical science and contribute to the development of ...

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention ... The Senior Development Scientist for Beckman Coulter Diagnostics is responsible for completing ...

Development Scientist I

Chaska, MN · On-site

$34 - $37/hr

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention ... The Development Scientist I is responsible for responsible for participating in development and ...

Senior Development Scientist

Chaska, MN · On-site

$105K - $115K/yr

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention ... The Senior Development Scientist for Beckman Coulter Diagnostics is responsible for completing ...

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How much do clinical development scientist jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for clinical development scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

How does a Clinical Development Scientist typically collaborate with cross-functional teams during a clinical trial?

Clinical Development Scientists play a central role in coordinating with various teams such as clinical operations, regulatory affairs, data management, and biostatistics throughout a clinical trial. They ensure that clinical protocols are scientifically sound and align with regulatory requirements, while also facilitating clear communication between departments to address study challenges and maintain timelines. By serving as the scientific point of contact, they help integrate input from multiple stakeholders, support troubleshooting during trial execution, and contribute to the preparation of study documents and data analysis.

What does a Clinical Development Scientist do?

A Clinical Development Scientist is responsible for designing, planning, and overseeing clinical trials that test new drugs, therapies, or medical devices. They collaborate with cross-functional teams to ensure that clinical studies are scientifically sound, compliant with regulations, and aligned with strategic objectives. Their work involves protocol development, data analysis, and interpretation of results to support regulatory submissions and product approvals. Ultimately, they play a key role in bringing safe and effective treatments to patients.

What is the difference between Clinical Development Scientist vs Clinical Research Associate?

AspectClinical Development ScientistClinical Research Associate
Required credentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's in Life Sciences or related field, often with certification in clinical trials
Work environmentDesigning and planning clinical trials, collaborating with teamsMonitoring clinical trials at sites, ensuring protocol compliance
Employer and industry usagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, CROs, research institutions
Common search and comparison intentUnderstanding roles in clinical developmentMonitoring and managing clinical trial sites

The Clinical Development Scientist focuses on designing, planning, and analyzing clinical trials, working closely with research teams. In contrast, the Clinical Research Associate primarily monitors trial sites to ensure compliance and data integrity. Both roles are essential in clinical research but differ in responsibilities and daily tasks.

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

To thrive as a Clinical Development Scientist, you need a solid background in life sciences, clinical research methodologies, and drug development, often supported by an advanced degree such as a PhD or PharmD. Familiarity with regulatory requirements, clinical trial management systems (CTMS), and data analysis tools is essential. Strong analytical thinking, attention to detail, and effective communication skills help you collaborate cross-functionally and drive successful clinical studies. These skills ensure rigorous study design, regulatory compliance, and effective advancement of new therapies through clinical pipelines.
More about Clinical Development Scientist jobs
What cities are hiring for Clinical Development Scientist jobs? Cities with the most Clinical Development Scientist job openings:
What states have the most Clinical Development Scientist jobs? States with the most job openings for Clinical Development Scientist jobs include:
Research Scientist

Full-time

Retirement, PTO

Posted 17 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!
Your Role: Clinical Development Scientist - Farm Animal
As a Clinical Development Scientist, you will lead the development and execution of global farm animal 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 target geographies.
Your Responsibilities:
• Lead the planning and execution of global farm animal 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.
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 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.
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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