Registered Vet Technician - Clinical Trials and Research Technician

University of GuelphGuelph, ON
Onsite

About The Position

This position is classified under the Grant and Trust Administrative & Technical Group. It is a temporary full-time role from 04/20/2026 to 06/30/2029. The role is for a Registered Veterinary Technician (RVT) with a passion for clinical research, contributing to studies that improve veterinary and human medicine. The position supports clinical trials and translational research at the OVC Health Sciences Centre (OVC-HSC), involving client-owned animals to advance animal and human health care. Responsibilities are dynamic, including hands-on patient care, clinical trial coordination, and research administration. The role requires strong initiative, problem-solving skills, and the ability to work both independently and collaboratively.

Requirements

  • A Registered Veterinary Technician in good standing with the OAVT, with completion of the VTNE and mandatory ethics exam.
  • A minimum of 2 years’ prior experience working as a Registered Veterinary Technician.
  • Experienced in blood collection, anesthesia monitoring, and patient handling.
  • Detail-oriented with strong organizational and data management skills.
  • Excellent communication skills, capable of working with veterinary teams, researchers, and pet owners.
  • Willingness to work both in clinical and preclinical research environments with dogs and cats.
  • Experienced in Microsoft Office, electronic medical records, and data tracking systems.

Nice To Haves

  • Previous experience in clinical research or veterinary clinical trials.
  • Undergraduate degree or experience with technical writing or publishing.
  • Interest in obtaining Registered Laboratory Animal Technician (RLAT) certification (training and support provided).

Responsibilities

  • Identify, screen, and recruit potential study candidates
  • Obtain informed consent from owners and ensure compliance with study protocols.
  • Assist in diagnostic and surgical procedures, including sedation monitoring, chemotherapy administration, and novel therapeutics.
  • Collect and process laboratory specimens (blood, urine, aspirates, tissues, etc.).
  • Monitor hospitalized study patients, including infusions and diagnostic imaging follow-ups.
  • Manage study logistics, including patient scheduling, imaging coordination, and follow-ups with study participants and veterinary clinics.
  • Managing clinical data collection and organization for both prospective and retrospective studies.
  • Prepare study materials, reports, and presentations for research meetings.
  • Coordinating with external clinics and research teams to ensure proper study documentation and patient status tracking.

Benefits

  • Protective rabies titre required.
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