In Vivo Research Associate I, II, or III
- Administer test substances using routes such as oral gavage, SQ, IV, ID, and topical ocular dosing across multiple species.
- Observe, monitor, and assess animal health and welfare.
- Perform biological specimen collection, including blood draws and tissue sampling from various laboratory species.
- Execute study tasks in compliance with GLP regulations, study protocols, SOPs, and company policies.
- Perform Intraocular Pressure (IOP) measurements using Pneumatonometer or Tonovet.
- Restrain and handle animals for ophthalmic imaging and diagnostic assessments.
- Assist with necropsies and ophthalmic tissue collections.
- Support surgical procedures and provide assistance to the operating surgeon.
- Perform and monitor anesthesia and analgesia, including post-operative recovery.
- Conduct study setup activities including room preparation, supply staging, and tube labeling.
- Perform aseptic techniques and follow biosafety and animal care guidelines.
- Place catheters in small and large animals as required by study design.
- Maintain accurate, timely data entry in internal systems including eQCM, Provantis, and Vivarium+.
- Perform other duties as directed by Management.
- In Vivo Research Associate I: Associate degree in veterinary technology with 1-2 years of experience, or BS with 1 year of experience.
- In Vivo Research Associate II: Associate degree in veterinary technology with 3 years relevant experience, or BS with 2 years of experience.
- In Vivo Research Associate III: Associate degree in veterinary technology with 4 years relevant experience, or BS with 3 years of experience.
- A combination of education and relevant hands-on experience will be considered.
- Registered Veterinary Technician (RVT) certification is highly desired, particularly for candidates with anesthesia, surgical support, or ophthalmic procedure experience.
- Prior experience in ophthalmology, in vivo models, or preclinical research.
- Working knowledge of animal handling, dosing techniques, clinical observations, and specimen collection.
- Strong attention to detail, documentation accuracy, and ability to follow strict regulatory procedures.
- Excellent communication skills and the ability to thrive in a collaborative, fast-paced environment.
- Strong work ethic, self-motivation, and ability to adapt to a dynamic team environment.
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