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Veterinary Clinical Research Associate Jobs (NOW HIRING)

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...

Icon plc

Senior Clinical Research Associate

Houston, TX · Hybrid

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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Veterinary Clinical Research Associate information

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$12

$31

$55

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

As of Jul 5, 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.
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Veterinary Clinical Research Associate jobs near you
Infographic showing various Veterinary Clinical Research Associate job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Clinical Research Associate/Monitor

Futran Tech Solutions Pvt. Ltd.

Remote

Contractor

Posted 22 days ago

Job description

Job Title: Clinical Research Associate/Monitor
6 months contract to perm
Work location: REMOTE
Required 30%-50% traveling
Candidate home location: required within DC, VA, MD only (a candidate needs to reside in DC, VA, MD)
Multiple Regional CRAs: 5 openings
USC/GC required
Search Term: Regional CRA, Contract CRA, Sr. CRA, Home-based CRA, Regional Clinical Research Associate, Regional CRA III, Sr. Clinical Research Associate, Senior Clinical Research Associate, Monitor, Contract CRA II, CRA III, Regional Monitor, Home-based Regional CRA, CRA, Contract Clinical Research Associate, Regional CRA Consultant, Phase I, Study Monitor, Contract Monitor, CRA, Research Associate
Multiple Studies with Health patients - Previous Phase I experience required
Contract CRAs, regional based with strong monitoring skills, minimum 3-5+ years monitoring experience within the pharmaceutical industry required traveling of minimum of 50% traveling to 1-2 sites within the same state as required. Require 100% commitment and contractors paid hourly. Therapeutic areas can range and candidates will be expected on working on about 6-8 protocols (max at 10 protocols) with different indications. Multiple sites and candidate has to be local to DC, VA, and MD areas.
Minimum 3-5+ years of CRA / Monitoring experience required
Start date is ASAP
TRAVEL INFORMATION FOR CANDIDATES -
The client is working to ensure candidates are as close as possible to their sites. Company is constantly adding new studies to the monitoring project. Monitors may be asked to take on additional sites closer to their home (or maybe a bit further then what they currently have) - they will work to keep travel as regionally located as possible. There are multiple sites in each region (depends on the allocation of the individual CRAs)
In addition they should be very clear about their monitoring experience showing that they are a Regional CRA/monitor currently. (I would say 3 years monitoring experience with Oncology study required) Candidates need to allocate 50% to 100% of their time to this assignment, preferred candidates home is close to the site locations (listed above).The CRA/Study Monitor designated activities include site visits, trial monitoring, tracking, documentation, collection, solicitation and review of (e) CRFs and submit data, preparation of reports, regulatory review and participation in teleconferences. Approximately 50% travel will be required, as the CRA Study Monitor's primary responsibilities will be monitoring of study sites.
Requirements
A strong healthcare background with at least 1-2 years prior monitoring Oncology study experience is required. Phase I research experience as a monitor, auditor, research coordinator, research associate or similar oncology research experience is required. The CRA/Study Monitor must hold a Bachelor's degree from an accredited college or University or be a grad from an accredited school of nursing.
Requirement:
  • 2+ years prior monitoring Oncology study experience is required. preferred. Phase I-IV research experience as a monitor, clinical research associate experience is required.
  • BS/BA in life sciences or health-related discipline, BSN, Bachelor of Science - Nursing, Pharmacy is highly desirable.
  • Minimum 3-5+ years clinical research monitoring experience including years in Phase I studies.
  • Strong working knowledge of GCPs, ICH Guidelines, and FDA Regulations
  • Ability and willingness to travel up to 50 % of the time, including minimum overnight stays travel as necessary
  • Experience with regulatory document review/collection and IRB submissions (including OHRP regulations), a plus
  • Experience with using a Trial Master File, a plus.

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