Senior Clinical Pharmacologist (Oncology)

AbbVieNorth Chicago, IL
$109,500 - $208,500

About The Position

Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical Pharmacology and Pharmacometrics (CPPM) goals. Generate new PK/PD proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques in PK/PD field. Act as a lead PK scientist in his/her area of expertise and critically evaluate relevant Clinical Pharmacology, PK/PD and regulatory advances and integrate this knowledge into research or development programs.

Requirements

  • PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Master’s Degree or equivalent education and typically 8+ years of experience, Bachelor’s Degree or equivalent education and typically 10+ years of experience; (relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
  • Excellent interpersonal skills
  • Ability to interact externally and internally and perform in a team setting
  • Demonstrates scientific acumen and has technical skills to perform the role
  • Persistent and resilient finds the way to move good ideas forward
  • Uses mistakes, failure and reflection as vehicles for learning and improvement
  • Delivers business results while also positioning AbbVie for long-term success
  • Connects unrelated concepts, generates original or unique ideas
  • Influences colleagues to achieve cross-functional alignment

Responsibilities

  • Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy.
  • Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports, relevant section of investigator brochures, common technical documents, white papers, and other similar documents.
  • Conduct data analyses including non-compartmental analyses, modeling and simulation, literature data analyses.
  • Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, Journal club.
  • Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a unified clinical pharmacology position to clinical, CMC and regulatory teams.
  • Author scientific publications and present at scientific conferences.

Benefits

  • paid time off (vacation, holidays, sick)
  • medical/dental/vision insurance
  • 401(k)
  • long-term incentive programs
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