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Associate Director of Pathology

Job in Carlsbad, Tom Green County, Texas, 76934, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-02-19
Job specializations:
  • Healthcare
  • Research/Development
Salary/Wage Range or Industry Benchmark: 150000 - 200000 USD Yearly USD 150000.00 200000.00 YEAR
Job Description & How to Apply Below
Location: Carlsbad

Role Summary

Associate Director of Pathology within the Preclinical Development Department, responsible for strategic scientific leadership in the assessment of nonclinical safety of candidate medicines. Collaborates with cross-functional teams to design nonclinical studies, provide regulatory input, and communicate findings to governance bodies and external stakeholders.

Responsibilities
  • Conduct histopathology review of internal and outsourced non-GLP and GLP research, pharmacology, and toxicology studies and provide interpretation that integrates all study data
  • Serve as nonclinical safety representative on cross‑functional project teams based on interest
  • Contribute to the design of non‑GLP and GLP nonclinical studies
  • Provide strategic input on the nonclinical toxicology and regulatory approach for IND‑enabling packages and for clinical stage programs
  • Author nonclinical sections of regulatory documents (e.g. IB, IND, NDA, DSUR, etc) and represent Ionis in meetings with regulatory authorities
  • Assess mechanism(s) of toxicity to determine clinical relevance and impact
  • Communicate pathology and nonclinical safety findings, interpretation, and impact to teams and governance committees
  • Represent Ionis externally (e.g. at scientific meetings and/or through participation in industry consortia, working groups, and/or professional societies)
  • Publish findings in high impact peer‑reviewed journal
Qualifications
  • Required:

    DVM (or equivalent)
  • Required:

    PhD in pathology, toxicology, or related life sciences discipline
  • Required:

    Board‑certification in anatomic pathology (e.g. ACVP, ECVP)
  • Required:

    At least 5 years of experience in toxicologic pathology of multiple species in the pharmaceutical or biotechnology field with a focus on IND‑enabling packages and beyond
  • Preferred:
    Experience with digital pathology and image analysis
  • Required:

    Experience with regulatory submissions and interactions
  • Required:

    Demonstrated strong decision‑making and problem‑solving skills
  • Required:

    Team player with proven interpersonal and communication skills
  • Required:

    Dedication to lifelong learning and professional development
Education
  • DVM (or equivalent)
  • PhD in pathology, toxicology, or related life sciences discipline
  • Board‑certification in anatomic pathology (e.g. ACVP, ECVP)
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Position Requirements
10+ Years work experience
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