A

AbbVie

Global biopharmaceutical company developing medicines

Value & Access Manager

Full-TimePosted on 10/19/2026
No salary listed
Mid
Bachelor's
Sydney NSW, Australia
HybridThree office days per week: Tuesday, Wednesday and Thursday.
Biology & BiotechRegulatory & Quality (Life Sciences)

About the job

Requirements
  • Tertiary qualifications in Biomedical, Science, Public Health, Health Economics, or Business Administration.
  • Experience in market access, health economics, or related roles within the pharmaceutical industry.
  • Understanding of the Australia and New Zealand healthcare system and reimbursement processes.
  • Experience in market access strategy development and advanced capability in writing high-quality health technology assessment submissions with clear, evidence-based value propositions.
  • Ability to lead projects independently, including management of external vendors and project timelines.
  • Ability to identify and understand complex issues and problems, interpret information, and provide appropriate recommendations across functional areas.
  • Written and verbal communication skills, including the ability to tailor content to technical and non-technical audiences.
  • Ability to work effectively in cross-functional teams and matrix environments.
  • Ability to adapt to evolving customer needs and demands within a changing environment.
  • Willingness to occasionally participate in business meetings outside standard working hours.
Responsibilities
  • Prepare Pharmaceutical Benefits Advisory Committee, Medical Services Advisory Committee, and PHARMAC submissions, including writing clear, evidence-based content and ensuring quality, alignment, and delivery timelines.
  • Serve as the market access lead on cross-functional teams, providing reliable access and payer insights to shape strategy and inform business planning.
  • Contribute to reimbursement feasibility assessments for pipeline assets to support portfolio prioritisation and resource allocation.
  • Monitor the reimbursement and policy landscape in Australia and New Zealand and contribute to stakeholder engagement activities supporting access objectives.
  • Collaborate with regional and global teams to ensure local access insights inform evidence planning and support alignment on access and pricing strategy.
  • Provide input into reimbursement and pricing assumptions for financial planning cycles.
  • Represent AbbVie externally with the Department of Health, Medicines Australia, and relevant external experts as required.
  • Report adverse events within 24 hours in accordance with AbbVie policies and procedures.
  • Participate in AbbVie workplace health and safety programs, adhere to policies, and promote a safe work environment.
  • Adhere to AbbVie internal codes of conduct and compliance processes.
  • Perform other ad hoc duties, including administrative duties, as requested.

About the company

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company Size

10,001+

Company Stage

IPO

Headquarters

North Chicago, Illinois

Founded

1888

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Simplify Jobs

Simplify's Take

What believers are saying

  • Apogee acquisition closed in 2026, expanding AbbVie’s immunology pipeline beyond Skyrizi and Rinvoq.
  • EU approvals for RINVOQ and EPKINLY in September 2026 broaden ex-U.S. revenue.
  • JUVMO launches in October 2026, adding a fresh neuroscience revenue line.

What critics are saying

  • Humira, Skyrizi, and Rinvoq concentration keeps AbbVie exposed if immunology growth slows in 2027.
  • Niaspan antitrust MDL and Biocell ALCL settlements carried $1.7 billion litigation accrual by June 2026.
  • Generic ubrogepant and atogepant suits threaten Ubrelvy and Qulipta exclusivity within years.

What makes AbbVie unique

  • Skyrizi and Rinvoq anchor AbbVie’s post-Humira immunology franchise across 11 EU RINVOQ indications.
  • JUVMO’s September 28, 2026 FDA approval gives AbbVie first-in-class Parkinson’s D1/D5 therapy.
  • AbbVie pairs blockbuster cash flows with Apogee, Iambic, and Valkai deal-making.

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Benefits

  • Remote Work Options
  • Flexible Work Hours
  • Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

4%

1 year growth

5%

2 year growth

5%
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Healthcare stocks are rebounding in 2026, led by Merck and AbbVie. Merck shares have climbed 39% and AbbVie's 24%, against about 12% for the S&P 500. Merck's second-quarter revenue rose 5% to $16.6 billion, beating Wall Street estimates. Keytruda sales hit $8.4 billion, though the drug will likely lose patent exclusivity by 2028. A subcutaneous version, Keytruda Qlex, may help retain market share. Merck's forward dividend yield is 2.3%. AbbVie's revenue grew 10.2% to almost $17 billion, with adjusted earnings per share up 22.9% to $3.65. Skyrizi and Rinvoq sales each rose about 24%, and neither faces US competition until 2033 and 2037 respectively. AbbVie has raised its dividend for 54 straight years, including its time as part of Abbott Laboratories.

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