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Veterinary Clinical Trial Monitor Jobs (NOW HIRING)

Responsibilities Veterinary Clinical Trial Administration * Assists with all duties needed to ... monitoring, and administration of study drugs and placebo medications via IM, IV, PO, Sub-Q.

Responsibilities Veterinary Clinical Trial Administration * Assists with all duties needed to ... monitoring, and administration of study drugs and placebo medications via IM, IV, PO, Sub-Q.

Complete site initiation, start-up, monitoring, site management, and site/study close-out activities according to SOPs, work instructions, and policies. * Develop clinical trial documents such as ...

Clinical Trial Specialist

Cincinnati, OH Β· On-site

$32.25 - $44/hr

May develop clinical trial documents, such as monitoring plans, informed consent. * Implement of analytical risk-based monitoring model at the site level and to work with site to ensure timely ...

Clinical Trial Specialist

Cincinnati, OH Β· On-site

$32.25 - $44/hr

May develop clinical trial documents, such as monitoring plans, informed consent. * Implement of analytic risk-based monitoring model at the site level and to work with site to ensure timely ...

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Tracks, monitors and reports on study progress * Manages CRO and vendor budgets and invoicing ...

Clinical Trial Specialist

Cincinnati, OH Β· On-site

$32.25 - $44/hr

May develop clinical trial documents, such as monitoring plans, informed consent. * Implement of analytical risk-based monitoring model at the site level and to work with site to ensure timely ...

Clinical Trial Manager

Marlton, NJ Β· On-site

$95K - $115K/yr

Clinical Trial Manager Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing ... Monitor the quality of vendor deliverables, address quality issues with the appropriate team member ...

The Role The Clinical Trial Manager (CTM) will be a key contributor to the successful execution of ... Monitor CRO and vendor performance, identify potential issues, and escalate concerns to Clinical ...

Clinical Trial Associate

Manhattan, NY Β· On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... monitoring visit reports (initiation, routine monitoring, and close-out) Meetings & Cross ...

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Veterinary Clinical Trial Monitor information

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How much do veterinary clinical trial monitor jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for veterinary clinical trial monitor in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does a veterinary clinical trial monitor do?

A Veterinary Clinical Trial Monitor is responsible for overseeing the conduct of clinical trials involving animals to ensure that they comply with regulatory requirements, protocols, and good clinical practice standards. They monitor the progress of studies, verify data accuracy, ensure animal welfare, and act as a liaison between the study sponsor and the clinical site. Their role is crucial for maintaining the integrity of the trial and ensuring reliable and ethical results.

What are the key skills and qualifications needed to thrive as a veterinary clinical trial monitor?

To thrive as a Veterinary Clinical Trial Monitor, you need a background in veterinary science or a related field, experience with clinical research protocols, and knowledge of regulatory guidelines such as Good Clinical Practice (GCP). Familiarity with electronic data capture (EDC) systems, clinical trial management software, and certifications like ACRP or SOCRA are highly beneficial. Attention to detail, strong organizational skills, and effective communication are essential soft skills for this role. These competencies ensure that veterinary clinical trials are conducted ethically, accurately, and in compliance with regulatory standards, safeguarding animal welfare and data integrity.

What are some common challenges faced by veterinary clinical trial monitors during multi-site studies?

Veterinary Clinical Trial Monitors often encounter challenges such as ensuring protocol compliance across multiple study sites, maintaining consistent data quality, and coordinating communication among diverse veterinary teams. They must frequently travel to each site to conduct monitoring visits and address any discrepancies or issues promptly. Strong organizational skills and adaptability are essential, as each site may have different resources, staff experience levels, and patient populations, all of which can affect trial consistency and progress.

What is the difference between Veterinary Clinical Trial Monitor vs Veterinary Research Assistant?

AspectVeterinary Clinical Trial MonitorVeterinary Research Assistant
CredentialsVeterinary degree, clinical trial trainingVeterinary degree, research experience
Work EnvironmentMonitoring clinical trials, site visitsLaboratory, fieldwork, data collection
Employer & IndustryPharmaceutical companies, CROsResearch institutions, universities
Search & Comparison IntentMonitoring, compliance, clinical trialsResearch, data analysis, lab work

The Veterinary Clinical Trial Monitor primarily oversees clinical trials, ensuring compliance and data integrity at trial sites. In contrast, the Veterinary Research Assistant supports research activities through data collection and laboratory work. Both roles require veterinary credentials but differ in focus, with the monitor emphasizing trial oversight and the assistant focusing on research support.

What are popular job titles related to Veterinary Clinical Trial Monitor jobs?

For Veterinary Clinical Trial Monitor jobs, the most frequently searched job titles are:

Infographic showing various Veterinary Clinical Trial Monitor job openings in the United States as of September 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,169 per year, or $40 per hour.

Senior Clinical Trial Manager, Veterinary Medicine

Indianapolis, IN β€’ On-site

Other

Retirement, PTO

Posted 10 days ago


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

This position will function in the efficient and effective management and execution of clinical studies. The individual will be responsible for continuing to grow and develop capabilities in clinical trial implementation. The incumbent will coordinate, oversee, and monitor clinical studies needed for the registration of global products for Elanco. The individual will maintain an excellent working knowledge of government regulations and policies pertaining to clinical trials, VICH-GCP guidelines, company Standard Operating Procedures (SOPs), and assigned study protocols. The position will interact with US research scientists and the global research and development teams to gain regulatory approval of these products.

Your Role

Clinical Trial Manager, Veterinary Medicine

Your Responsibilities
  • Plan, manage, and oversee all phases of veterinary clinical trials, including study initiation, site recruitment and training, monitoring, execution, close‑out, and compliance with study protocols and SOPs.
  • Support high‑quality study delivery through protocol and final report review, data capture design, QA/audit responses, risk management, and continuous improvement of trial conduct and data quality.
  • Partner cross‑functionally with R&D, commercial teams, external partners, and clinical sites to ensure alignment, timelines, quality, and successful study execution.
  • Support regulatory and operational activities, including FDA/USDA inspections, communication with regulators, budgeting, contracting, invoicing, forecasting, and vendor selection and oversight.
  • Provide leadership and mentorship to study monitors and administrators while contributing to a high‑performing, innovative team culture aligned with Elanco values.
Minimum Qualification (education, experience and/or training, required certifications)

Education: Bachelor's degree in a science or health related field and 5+ years' experience in veterinary clinical trial management and execution of clinical studies.

Required Experience: Strong background in monitoring of veterinary clinical studies. Working knowledge of computer applications including electronic data capture system(s), MS Word, Outlook, Teams, Excel, PowerPoint, Adobe, and SMF applications. Required veterinary experience: Candidates must have direct experience managing and executing veterinary clinical trials. Experience limited to human clinical trials, general clinical operations, or adjacent regulatory/project management work will not meet this requirement.

Top 2 skills

Previous trial management experience in veterinary medicine. Proven ability to manage cross‑functional teams and collaborate with internal and external stakeholders, including regulatory bodies (FDA/USDA).

What Will Give You a Competitive Edge (Preferred Qualifications)

Has experience supporting FDA and USDA inspections and audits, ensuring trial compliance with GCP and regulatory requirements. Has led cross‑functional collaborations with R&D, commercial teams, and external partners to drive end‑to‑end clinical trial execution, including protocol development, budgeting, vendor oversight, and study management.

Location

Location: Indianapolis, IN – Hybrid Travel: Minimal 25%

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
  • 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.

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.

About Elanco

Elanco Animal Health Incorporated (NYSE: ELAN) is a global leader in animal health dedicated to innovating and delivering products and services to prevent and treat disease in farm animals and pets, creating value for farmers, pet owners, veterinarians, stakeholders, and society as a whole. With nearly 70 years of animal health heritage, we are committed to helping our customers improve the health of animals in their care, while also making a meaningful impact on our local and global communities. At Elanco, we are driven by our vision of Food and Companionship Enriching life and our Elanco Healthy Purposeβ„’ CSR framework – all to advance the health of animals, people and the planet. Learn more at www.elanco.com.

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