1

Veterinary Clinical Research Associate Jobs (NOW HIRING)

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of ...

Showing results 21-40

Veterinary Clinical Research Associate information

See salary details

$12

$31

$55

How much do veterinary clinical research associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for veterinary clinical research associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

What is the difference between Veterinary Clinical Research Associate vs Veterinary Technician?

AspectVeterinary Clinical Research AssociateVeterinary Technician
CredentialsBachelor’s degree in veterinary medicine or related field, often with research trainingAssociate’s or Bachelor’s degree in veterinary technology
Work EnvironmentResearch facilities, pharmaceutical companies, clinical trial sitesVeterinary clinics, animal hospitals, laboratories
Employer & IndustryPharmaceutical companies, research organizations, academiaVeterinary clinics, animal care facilities
Job FocusOverseeing clinical trials, ensuring protocol compliance, data collectionAssisting veterinarians, patient care, laboratory procedures

The Veterinary Clinical Research Associate primarily focuses on managing clinical trials and research studies in veterinary medicine, requiring research experience and specific certifications. In contrast, Veterinary Technicians support daily veterinary care and procedures. Both roles are essential in veterinary settings but differ significantly in responsibilities and work environments.

What does a veterinary clinical research associate do?

A Veterinary Clinical Research Associate (CRA) is responsible for overseeing and monitoring clinical trials involving veterinary medicines, treatments, or devices. They ensure that studies comply with regulatory requirements, protocols, and ethical standards while collecting accurate data on the safety and efficacy of veterinary products. Veterinary CRAs work closely with veterinarians, study sponsors, and regulatory agencies to ensure the success and integrity of clinical research projects. Their role often includes site visits, data verification, and preparing reports for regulatory submissions.

What are the key skills and qualifications needed to thrive as a veterinary clinical research associate, and why are they important?

To thrive as a Veterinary Clinical Research Associate, you need a strong background in veterinary science, animal health, and clinical research, often supported by a relevant degree and experience in veterinary or biomedical fields. Familiarity with Good Clinical Practice (GCP), regulatory compliance systems, and data management tools such as EDC (Electronic Data Capture) platforms is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for managing studies and collaborating with multidisciplinary teams. These skills and qualifications ensure accurate and ethical research, regulatory compliance, and the advancement of veterinary medicine.

What are the main challenges veterinary clinical research associates face when managing multi-site clinical trials?

Veterinary Clinical Research Associates (VCRAs) often encounter challenges in coordinating and standardizing procedures across multiple veterinary sites. Ensuring consistent protocol adherence, data collection, and communication between veterinary teams can be complex due to varying resources, workflows, and staff experience. VCRAs must be proactive in troubleshooting site-specific issues, training staff, and maintaining regulatory compliance. Strong organizational and interpersonal skills are essential to manage these dynamic environments and ensure the success of clinical trials.
More about Veterinary Clinical Research Associate jobs
What cities are hiring for Veterinary Clinical Research Associate jobs? Cities with the most Veterinary Clinical Research Associate job openings:
What are the most commonly searched types of Veterinary Clinical Research jobs? The most popular types of Veterinary Clinical Research jobs are:
What states have the most Veterinary Clinical Research Associate jobs? States with the most job openings for Veterinary Clinical Research Associate jobs include:
What job categories do people searching Veterinary Clinical Research Associate jobs look for? The top searched job categories for Veterinary Clinical Research Associate jobs are:
Infographic showing various Veterinary Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 11% Part Time, 2% Temporary, and 3% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Senior Clinical Research Associate

410 ICR United States USA

Blue Bell, PA • Remote

Full-time

Posted 21 days ago


Job description

Senior CRA

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Contractor Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month contract. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

  • Bachelor’s degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • Minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

#LI-Remote #LI-ZH1


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply