Lead Pharmacometrician — PK/PD Modeling & Strategy

BioSpace; North Chicago (IL); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Comprehensive benefits

Paid time off

Job summary

AbbVie is seeking a Pharmacometric Scientist to conceive, execute and communicate multi-disciplinary PK/PD modeling and simulations to support development plans and regulatory requirements across functions. Lead PK/PD modeling efforts and contribute to strategy while collaborating with Clinical Pharmacology teams.

You will author regulatory documents, present findings to leadership, and help advance projects through regulatory review, aligning with business objectives and scientific rigor.

Qualifications

• PhD with 3+ years of relevant field experience; advanced modeling and analysis.
• Excellent interpersonal skills and ability to interact with internal stakeholders.
• Strategic thinker with enterprise perspective and proven leadership.

Responsibilities

• Lead multi-disciplinary modeling, data analyses, and interpretation for programs.
• Assist Clinical Pharmacology senior management in selecting action plans.
• Author PK/PD analyses plans, study reports, population PK reports, exposure-response analyses reports, CTD/labels, and other regulatory documents.
• Represent Pharmacometrics in project teams and leadership meetings.
• Collaborate to develop a unified Clinical Pharmacology position.
• Author scientific publications and present at conferences.
• Participate in internal and external initiatives and working groups.

Skills

Excellent interpersonal skills

Strategic thinking

Enterprise view

Cross-functional collaboration

Leadership

Analytical skills

Education

PhD or equivalent in a relevant field

Master's Degree or equivalent

Bachelor's Degree or equivalent

Job description

AbbVie is seeking a Pharmacometric Scientist to conceive, execute and communicate multi-disciplinary PK/PD modeling and simulations to support development plans and regulatory requirements across functions. Lead PK/PD modeling efforts and contribute to strategy while collaborating with Clinical Pharmacology teams.

You will author regulatory documents, present findings to leadership, and help advance projects through regulatory review, aligning with business objectives and scientific rigor.