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Director, Clinical Pharmacology

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Council of State and Territorial Epidemiologists
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
  • Management
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

ICompany Description

Abb Vie'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 Abb Vie, please visit us at  Follow @abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok.

Job Description Purpose

Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management, regulatory agencies, and external peers. Leads strategic planning for drug development activities and projects to achieve departmental strategies, goals, and objectives. Utilizes scientific expertise to provide appropriate interpretation of data and relates implications of results to management. Serves as liaison to other departments/divisions for any study/project needs. Influences and strategically manages linkages across businesses and understands the impact of business decisions and solutions.

Leads teams within Clinical Pharmacology and Pharmacometrics and is accountable for effective performance of the teams.

Responsibilities
  • Independently leads Clinical Pharmacology/PK/PD activities and multiple major projects. Assists R&D senior management in the selection of action plans that best meets drug development business objectives.
  • Identifies issues impacting multiple complex projects and leads issue resolution. Conducts risk assessments and leads the function in development of contingency plans. Assures project remains in alignment with strategic objectives.
  • Provides overall timelines to assess portfolio opportunities. Negotiates with other functional areas on project outcomes and deliverables to meet conflicting demands (time, cost, quality/performance).
  • Provides expert scientific and strategic consultation to R&D, Regulatory, and all levels of management on critical decisions and development plans. Connects scientific, regulatory, and business implications from multiple teams. Influences and strategically manages linkages across businesses and understands the impact of business decisions and solutions.
  • Responsible for critically evaluating technical, scientific aspects of all Abb Vie projects along with Clinical Pharmacology management. Reviews clinical protocols and scientific reports for regulatory filings and anticipates regulatory questions. Leads Clinical Pharmacology regulatory documents writing, submission and response to regulatory agency comments.
  • Independently conducts due diligence assessments, summarizes results and represents Clinical Pharmacology on business development teams.
  • Identifies and develops process improvement initiatives and reviews recommendations with management for approval and sponsorship.
  • Responsible for leading efforts to develop departmental goals. Makes strategic PK/PD decisions for the department. Provides leadership on strategic clinical pharmacology and drug development.
  • Manages personnel including development, mentoring, and effective delegation.
  • Leads teams within department, across Clinical Pharmacology and across functions. Responsible for leadership of cross‑functional teams and accountable for effective performance of the team. Actively manages project team behaviors, mediates internal team disputes, and facilitates establishment of healthy and high‑performing teams.
Qualifications

This is a hybrid opportunity, 3x/week in the Lake County, IL

  • PhD with typically 9+ years of experience or Pharm D with typically 11+ years of experience in a relevant field, Master’s Degree in Science or related field with typically 17+ years of related work, Bachelor’s Degree in Science or related field with typically 19+ years or more of related work; (
    * relevant field includes experience with PK, PBPK, PK‑PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
  • Excellent interpersonal skills
  • Advanced knowledge and experience in multiple therapeutic and/or functional areas
  • Experience across range of development phases
  • Reco…
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