Lead Clinical Pharmacologist – PK/PD & Modelling

AbbVie; North Chicago (IL); On-site; USD 180,000 - 230,000; Full time

Job summary

AbbVie in North Chicago, IL, seeks a lead PK scientist to conceive and execute novel scientific research in Clinical Pharmacology that advances CPPM goals. You will generate PK/PD proposals, lead efforts, and evaluate regulatory advances to integrate knowledge into programs.

The role includes supporting Phase 1-4 studies, authoring regulatory documents, and collaborating across cross-functional teams to ensure a unified pharmacology position for regulatory submissions.

Qualifications

• PhD with 0 years of experience, or PharmD 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.

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.

Skills

Scientific acumen

Leadership

Collaboration

Education

PhD or PharmD

Master's degree

Bachelor's degree

Job description

AbbVie in North Chicago, IL, seeks a lead PK scientist to conceive and execute novel scientific research in Clinical Pharmacology that advances CPPM goals. You will generate PK/PD proposals, lead efforts, and evaluate regulatory advances to integrate knowledge into programs.

The role includes supporting Phase 1-4 studies, authoring regulatory documents, and collaborating across cross-functional teams to ensure a unified pharmacology position for regulatory submissions.