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    Pathologist, Director, Precision Medicine Pathology - South San Francisco, United States - AbbVie

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    Full time
    Description

    Company Description

    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 immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us Follow @abbvie onTwitter,Facebook,Instagram,YouTubeandLinkedIn.
    Job Description

    Precision Medicine Pathology supports projects from Discovery through Companion Diagnostics across therapeutic areas. Pathologists are deployed to projects to provide expertise in humandisease pathology, experimental pathology support and contribute to the development andinterpretation of tissue-based assays.

    Specific responsibilities can include:

    Contribute to or lead efforts to identify tissue-based biomarkers, including their

    characterization, validation and use in the development of tissue-based assays.

    Contribute to or lead the design and interpretation of tissue-based studies investigating

    aspects such as target biology, drug MOA, target pathway activation, pharmacodynamic

    effects, biomarker prevalence, or drug distribution.

    Contribute to the design, validation and deployment of pathology assays, including the

    determination of assay parameters such as specificity and sensitivity.

    Develop, validate and implement scoring paradigms for tissue-based assays

    Design, implement and oversee pathology-based biomarker and diagnostic testing,

    including data analysis:

    o Direct the development, outsourcing and validation of clinically applicable tissue-based

    assays. Assist in the development of assay protocols as needed.

    o Write the relevant pathology-based biomarker and diagnostics testing sections in drug

    development and registration documents such as clinical study protocols, clinical study

    reports, investigator brochures, and regulatory submission packages (INDs, NDAs,

    BLA's).

    Provide pathology input to project teams and ensure access to state-of-the-art tissue-based

    techniques and samples for target pathway evaluation in human disease:

    o Implement technologies and/or methodologies via a combination of in-house efforts

    and the use of CROs or other external expertise using techniques such as in situ

    hybridization, immunohistochemistry (including multiplexed), image analysis, RNAseq,

    qPCR, etc.

    o Evaluate the scientific basis and clinical applicability of the proposed assays, their

    validation status and any related technical issues.

    o Assume responsibility for the assessment and scoring of specimens and the preparation

    of reports summarizing the data, analysis and interpretation of findings.

    o Collaborate with project teams from concept to reagent generation to quantitation and

    approval plan for CDx as needed.

    Participate in the evaluation of external licensing or collaborative opportunities (including

    CDx collaborations) and oversee internal components of shared programs.

    Participate in or lead project development teams or sub-teams. Coordinate with

    appropriate team members to advance projects efficiently.
    Qualifications

  • Experienced pathologist (MD, DVM) with relevant post-doctoral academic, clinical and/or industry pathology experience -required
  • Board certification in pathology (anatomic, clinical, combined, with or without additional specialization) - required
  • PhD in relevant field of science -preferred, but not required
    Additional Information
    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 ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay 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/visioninsurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.
  • This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable.The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law. AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.


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