Senior Principal Pathologist

About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Job Description The primary function is to assess the safety of experimental compounds by evaluating their effects across available nonclinical safety models. Act as a scientific subject matter expert for preclinical safety data for other AbbVie departments as a member of cross-functional project teams. Develop and conduct those portions of study protocols that deal with anatomic and clinical pathology including not only the collection and evaluation of data regarding gross, microscopic, ultra-structural, and clinical pathology but, lastly, the preparation of comprehensive reports correlating these data. Integrate data sourced from in vivo studies as well as in vitro models and in silico predictions to generate a comprehensive safety assessment for early drug development programs.

Provide scientific expertise to scientific staff of other departments as a member of cross-functional teams. In cooperation with the Toxicology Department, design, direct, and evaluate in vivo studies to determine the potential toxicity of experimental compounds in different species of animals. This includes advanced endpoints (molecular pathology, ultrastructure, imaging, -omics, etc) Integrates the anatomic pathology data, clinical pathology data and other study findings to generate a pathology report as a component of the Toxicology report. Partner with toxicologists, pathologists and other functions to develop optimal strategies to address specific toxicology issues as well as select and advance Development compounds. Ability to function in multidisciplinary teams to address regulatory queries. Serves and/or leads issue resolution teams and participates in due diligence teams. Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Qualifications Doctor of Veterinary Medicine (DVM or equivalent) plus post graduate training in veterinary pathology. Board Certification in Veterinary Anatomic Pathology (ACVP or equivalent) strongly preferred. Candidates with a Ph.D. in pathology or related discipline are strongly preferred. Familiarity with related fields: pharmacology, toxicology and drug development. Seasoned experience in biological research, supervisory abilities, and the ability to work effectively with other people. Excellent oral and written skills with a proven record of scientific contributions to the scientific community. At least 5-15 years of experience as a veterinary pathologist in the pharmaceutical business is required.

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​ This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be