Head, Global Oncology Pipeline, Medical Affairs

AbbVie

Illinois

On-site

USD 250,000 - 450,000

Full time

14 days+

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Benefits offered by this job

Medical/dental/vision insurance
401(k) with company match
Long-term incentive programs

Job summary

AbbVie is seeking a senior Medical Affairs leader to drive global strategy and evidence plans across US and international markets, with emphasis on oncology/hematology. You will lead cross-functional teams, shape pipeline governance, and influence commercialization strategies from discovery onward.

The role requires deep scientific acumen, strong leadership, and the ability to translate complex data for diverse stakeholders across the enterprise.

Qualifications

  • MD or equivalent advanced degree in a relevant scientific discipline (e.g., oncology/hematology).
  • 15+ years of experience in the pharmaceutical or biotechnology industry with a focus on oncology/hematology.
  • Proven expertise in clinical development, regulatory requirements, and commercialization of oncology therapies.
  • Demonstrated leadership in medical affairs, including managing direct and indirect reports and cross-functional teams.
  • Strong scientific knowledge of solid tumor biology, clinical trial design, biomarkers, and emerging modalities (immuno-oncology, targeted therapies).
  • Excellent collaboration and communication skills for cross-functional stakeholder engagement.

Responsibilities

  • Lead and oversee pipeline medical strategy and value/evidence planning across disease areas for US and International markets.
  • Drive differentiation of medical, value and evidence strategies from discovery through pre-launch and launch.
  • Coordinate across therapeutic areas to align TA-level pipeline strategies into a cohesive AbbVie plan.
  • Integrate insights from HCPs, patients, and payors into development and commercialization programs.
  • Co-create brand strategy for assets with embedding of US and international market insights.
  • Represent medical affairs in pipeline governance and serve as the point of contact for commercial and development teams.
  • Oversee resource management and staffing across the lifecycle, including early discovery to inline teams.
  • Ensure smooth handover to US and international launch teams and minimize duplication of effort.
  • Lead integrated evidence planning and collaboration with Value and Evidence teams.

Skills

Medical affairs leadership
Scientific presentation
Cross-functional collaboration
Strategic thinking
Effective communication

Education

MD or equivalent advanced degree (oncology/hematology)

Job description

Company Description
About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

*Hybrid 3x per week in Lake County, IL, Florham Park, NJ or San Francisco, CA.

Purpose
  • Lead global pipeline medical affairs strategy and develop compelling differentiation across the lifecycle, leveraging distinctive insights from the market to shape AbbVie TA pipeline
  • Shape initial value and evidence strategy and initiate Ev Gen plans, leveraging insights from payors, patients, and physicians. Direct pipeline execution team, ensuring pull through of strategy to Enterprise Research MSLs
  • Collaborate with counterparts in International TAs, Global Therapeutic Area BU and Development
  • Represent TA in pipeline governance, where aligned with TA BU Head
  • Interface with Operations and Medical Engagement teams to operationalize pipeline strategy
Responsibilities
  • Lead and oversee pipeline (including BD) medical, value and evidence strategy development across all disease areas within TA to serve both US and International markets for all indications/ brands up to 24-36 months pre-launch (in any geography)
  • Drive compelling differentiation of medical, value and evidence strategy from discovery, leveraging distinctive insights from US and International markets
  • Coordinate across TAs to ensure that TA-level pipeline strategies coalesce into a coherent AbbVie pipeline strategy
  • Ensure HCP, Patients and Payor insights are incorporated into the developments programs to accelerate and differentiate clinical and commercialization strategies (e.g., streamlined patient data collection, patient finding)
  • Co-create the Brand strategy for all assets and ensure US and International market insights are embedded in the brand strategy
  • Represent medical affairs in pipeline-related governance, serving as the single point of contact for commercial and development counterparts
  • Serve as final decision maker (pre-BU head) for all pipeline-related strategy and decisions
  • Manage pipeline resources effectively, redirecting pipeline team to enterprise critical assets along the lifecycle as needed, starting as early as discovery
  • Ensure effective handover to US and International inline/ launch teams, onboarding with relevant TAs to share insights/ approach/ etc. from pipeline strategy efforts and minimizing duplication of effort across pipeline and inline teams
  • Lead cross-functional gap assessment and Integrated Evidence Planning (IEP) and collaborate with Value and Evidence
  • Define strategy for enterprise researchMSLsin US and affiliates, leveraging pipeline insights to develop priorities and shape tactical plans
  • Coordinate with pipeline execution group in US Medical Engagement to drive execution
  • Collaborate with US Medical Engagement to track impact-focused KPIs and re-shape pipeline strategy based on impact or best practices
Qualifications
  • M.D., or equivalent advanced degree in a relevant scientific discipline (e.g., oncology/hematology)
  • 15+ years of experience in the pharmaceutical or biotechnology industry, with a focus on oncology, specifically hematology
  • Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies
  • Proven leadership experience in medical affairs, including managing direct and indirect reports, cross-functional teams and influencing strategic direction at the senior executive level
  • Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities (e.g., immuno-oncology, targeted therapies, precision medicine)
  • Proven ability to work cross-functionally and collaborate effectively with clinical development, regulatory, commercial, and other business functions
  • Exceptional communication skills, with experience presenting complex scientific information to both technical and non-technical stakeholders
Preferred Qualifications
  • Familiarity with advanced cancer treatment modalities such as CAR-T therapies, combination therapies, and immuno-oncology
  • Strong publication and scientific communication track record in oncohematology, including contributions to peer-reviewed journals and major oncology conferences
  • Experience in managing global medical affairs activities across multiple geographic regions (focus on Global strategy and US region)
Physical Requirements
  • Ability to travel domestically and internationally (up to 25-30%).
Additional Information
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the timeof this posting based on the job grade for this position.Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in thefuture.

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision insurance and 401(k) to eligible employees.

  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employer remains in the Company’s sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

What AbbVie Has to Offer

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

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