AbbVie logo

Senior Director, Pipeline Market Access Strategy - Oncology

AbbVie

Mettawa, ILOnsitePosted 2 days agoUSD 206,500 - USD 393,000 yearly
Full TimeDirector & AboveCommercial & Pharma SalesPharmaceutical
Original posting ↗

Summary

The Senior Director, Pipeline Market Access Strategy (PMAX) is a newly created role responsible for leading and inspiring the end-to-end global market access strategy for pipeline assets within their assigned Business Unit. This position will require strong enterprise leadership to navigate the organization through multiple external environment pressures on global pharmaceutical pricing and reimbursement. This role bridges early asset development and future commercialization readiness, ensuring that pricing and access considerations are embedded from the earliest stages of the drug development lifecycle and through Phase 3 design and identification of evidence needs.

Job description

Key Responsibilities

Pipeline Access Strategy & Portfolio Leadership

  • Owns the end-to-end pipeline Integrated access strategy for all pre-launch and development-stage assets within the assigned Business Unit, ensuring strategies are comprehensive in addressing evidence needs, policy considerations, pricing potential, and commercial considerations.
  • Serves as the primary voice of pipeline market access strategies at Business Unit governance forums, including LMG, TASC, CSM, ASTs, and other senior leadership reviews.
  • Serves as the voice of access into pipeline Business Development opportunities.
  • Leads prioritization exercises across the pipeline portfolio to ensure resources and strategic attention are allocated to assets with the greatest near- and long-term access complexity and business impact.
  • Creates and optimizes launch strategies inclusive of considerations for IRA, MFN, and other market forces (US Channel dynamics).
  • Defines and delivers the Access Roadmap—a cross-functionally developed strategy that articulates the access approach for each pipeline asset by development phase, anticipated launch timing, and global evidence deliverables.

Early Development Integration

  • Partners with R&D and Regulatory teams to embed access-relevant endpoints, comparators, and trial design elements into clinical development programs from Phase I/II onward.
  • Defines and champions Target Product Profiles (TPPs) from a market access perspective, translating payer value requirements into actionable clinical and evidence generation guidance for asset teams.
  • Generates and maintains global payer and HTA evidence requirements across major markets (US, EU5, Japan, and emerging markets).

US & International Strategy Alignment

  • Provides strategic leadership and direction to the US Pipeline Strategy Lead and International Pipeline Strategy Lead.
  • Aligns US payer strategy, formulary positioning, and value communication frameworks with international HTA, pricing, and reimbursement approaches.
  • Anticipates cross-market reference pricing dynamics, parallel trade risks, and HTA precedent effects.
  • Partners closely with US and International Pipeline Strategy Leads to develop and execute a structured pipeline-to-launch transition framework.
  • Collaborates with US and international commercial, medical, and market access teams to ensure seamless knowledge transfer and strategic handoff at the point of regulatory approval.
  • Leads cross-functional launch readiness reviews in partnership with US and International teams to identify and resolve access gaps prior to approval.
  • Ensures that affiliate and in-country market access teams are equipped with globally aligned value messages, health economic tools, and reimbursement dossiers well in advance of launch.

Cross-Functional Leadership & Partnership

  • Provides strategic direction and partnership to cross-functional groups including HEOR, R&D, Regulatory, Global Commercial Development, Global Marketing, Government Affairs, and Business Development.
  • Leads the development of Integrated Evidence Plans (IEPs) in close collaboration with HEOR.
  • Partners with Government Affairs to anticipate and shape the evolving policy and reimbursement landscape.
  • Collaborates with Global Commercial Development and Global Marketing to ensure pipeline access strategies are aligned with brand positioning, indication sequencing, and long-range commercial forecasts.

Business Development & Asset Evaluation

  • Works closely with Business Development to inform the market access potential of in-licensing, partnership, and acquisition opportunities.
  • Establishes and communicates access-based licensing priorities.
  • Serves as the access subject matter expert in due diligence processes.

Governance, Stakeholder Engagement & People Leadership

  • Represents pipeline market access priorities at senior leadership governance forums, portfolio review committees, and cross-Business Unit strategy sessions.
  • Builds, develops, and retains a high-performing pipeline access team, providing mentorship, career development, and performance management.
  • Fosters a culture of innovation, rigor, and affiliate-centricity within the pipeline access team.

Qualifications

An advanced degree (MBA, MPH, PhD, PharmD, or equivalent) in business, health economics, public policy, life sciences, or a related field is required. Formal training or demonstrated expertise in health technology assessment (HTA), health economics, outcomes research, or pharmaceutical development is strongly preferred. Bachelor's degree in a scientific, business, or public health discipline is required as a minimum baseline.

A minimum of 12–15 years of progressive, senior-level experience in market access, pricing, reimbursement, HEOR, or a closely related pharmaceutical/biopharmaceutical function — with a substantial portion of that experience focused on pipeline and pre-launch strategy. Demonstrated expertise in global market access, including a deep working knowledge of HTA processes, payer evidence requirements, pricing and reimbursement frameworks, and access decision-making dynamics across major international markets. Proven experience shaping clinical development strategy from a market access and outcomes evidence perspective. Strong track record of leading and developing high-performing teams in a matrixed, multinational environment. Experience supporting Business Development activities is highly preferred. Experience across multiple therapeutic areas is an asset, though deep expertise in at least one is required.

Requirements

  • Advanced degree (MBA, MPH, PhD, PharmD, or equivalent) in business, health economics, public policy, life sciences, or related field
  • Bachelor's degree in scientific, business, or public health discipline
  • Minimum 12–15 years progressive senior-level experience in market access, pricing, reimbursement, HEOR, or related pharmaceutical function
  • Substantial experience focused on pipeline and pre-launch strategy
  • Deep working knowledge of HTA processes, payer evidence requirements, pricing and reimbursement frameworks across major international markets
  • Proven experience shaping clinical development strategy including clinical trial design, endpoint selection, and Integrated Evidence Plan development
  • Strong track record leading and developing high-performing teams in a matrixed, multinational environment
  • Ability to influence cross-functional partners without direct authority
  • Comfortable operating at senior leadership level and communicating complex access strategy to executive audiences
  • Deep expertise in at least one therapeutic area
  • Formal training or demonstrated expertise in HTA, health economics, outcomes research, or pharmaceutical development (preferred)
  • Experience supporting Business Development activities including asset due diligence, licensing evaluations, and access-based valuation assessments (preferred)
  • Experience across multiple therapeutic areas (preferred)

Benefits

  • Paid time off
  • Medical, Dental & Vision
  • 401(k)
  • Long-term incentive programs

Company overview

AbbVie is a global biopharmaceutical company that discovers, develops, and markets advanced therapies for some of the world's most complex and serious diseases. Founded in 2013 as a spin-off from Abbott Laboratories, AbbVie has established itself as a leader in immunology, oncology, neuroscience, eye care, and virology. The company's flagship product, Humira (adalimumab), was one of the world's top-selling drugs for treating autoimmune conditions like rheumatoid arthritis and Crohn's disease. AbbVie maintains a robust pipeline of innovative medicines and has expanded its portfolio through strategic acquisitions, including Allergan in 2020. With research facilities across the United States and globally, AbbVie focuses on advancing science to improve patient outcomes while maintaining strong commercial operations worldwide. The company operates with a patient-centric approach and invests significantly in research and development to address unmet medical needs across multiple therapeutic areas.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.