Veterinary Clinical Pathologist (Remote)

CareAbout•Overland Park, KS

34d•$160,000 - $200,000•Remote

About The Position

Veterinary Clinical Pathologists will serve as a Clinical Pathologist on nonclinical safety studies. The critical and main function of the position will be interpreting data and writing clinical pathology reports (GLP and nonGLP), collaborating with Study Directors and Anatomic Pathologists, and other relevant personal. This is a North America based remote position.

Requirements

D.V.M. (or Equivalent as listed by AVMA ECFVG) required
MS/MVSc/MSc, and/or Ph. D. preferred
Minimum 1-4 years experience as a Veterinary Clinical Pathologist, ideally with pharma, biotech, and/or CRO experience.
DVM, Diplomate ACVP, JCVP, ECVP in Veterinary Clinical Pathology
Ability to utilize Microsoft Office and pathology data management systems.
Proficiency in both written and verbal English; ability to read, analyze, and interpret common scientific and technical journals; ability to respond to common inquiries or complaints from customers or regulatory agencies; and, ability to effectively present information to clients, management, and public groups.
Ability to utilize appropriate mathematical concepts for interpreting scientific studies.
Training needs for this position may include continuing education in toxicology and pathology.
Continual GLP training.
Additional skills required include, but are not limited to: general reading, writing, and verbal communication skills; and skills in scientific writing or electronic publishing.

Nice To Haves

demonstrates expertise in clinical pathology
demonstrates knowledge of current scientific and industry specific literature
ability to successfully operate independently with minimal guidelines
has excellent interpersonal and communication skills

Responsibilities

Evaluate clinical pathology data and prepare reports for nonclinical safety studies.
Support Study Directors in addressing clinical pathology related data and issues with sponsors.
Support client development through discussions with sponsors about study goals and designs.
Implement/support company-wide scientific initiatives involving the Clinical Pathology department as assigned.
Support continuing development of Study Directors and other Safety Assessment personnel.
Other duties as assigned