Global Market Access Director, Specialty Pipeline

AbbVie; Mettawa (IL); On-site; USD 207,000 - 393,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie Inc. is seeking a Senior Director, Pipeline Market Access Strategy to lead end-to-end global access for obesity, eye care, and related therapies.

The role requires directing access strategy across pre-launch and development stages, with emphasis on payer evidence, pricing, and policy alignment. You will lead a team across US and international markets, partnering with R&D, Regulatory, HEOR, and Government Affairs to shape clinical development and evidence plans for successful launches and

Qualifications

• Minimum 12–15 years of senior-level market access experience.
• Deep working knowledge of HTA processes, payer evidence requirements, pricing and reimbursement frameworks.
• Proven ability to shape clinical development strategy from a market access perspective.
• Experience leading and developing high-performing teams in a matrixed environment.

Responsibilities

• Owns the end-to-end pipeline market access strategy for pre-launch and development-stage assets.
• Leads cross-functional teams across HEOR, R&D, Regulatory, Global Commercial Development and Government Affairs.
• Develops and guides Integrated Evidence Plans (IEPs) with HEOR for payer evidence needs.
• Partners with US and International teams to align domestic and global access strategies.
• Shaping pricing, access and evidence generation to support global launch readiness.

Skills

Market access strategy

HTA expertise

Leadership

Clinical development partnership

Cross-functional collaboration

Education

MBA/ MPH/ PhD/ PharmD

Bachelor's degree

HTA/outcomes research training

Job description

AbbVie Inc. is seeking a Senior Director, Pipeline Market Access Strategy to lead end-to-end global access for obesity, eye care, and related therapies.

The role requires directing access strategy across pre-launch and development stages, with emphasis on payer evidence, pricing, and policy alignment. You will lead a team across US and international markets, partnering with R&D, Regulatory, HEOR, and Government Affairs to shape clinical development and evidence plans for successful launches and