Director, HEOR Strategy - Dermatology

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 at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

he Director, HEOR is accountable for the development, alignment, and delivery of HEOR strategy and evidence-generation initiatives for assigned on-market and/or pipeline indication(s). Serving as the HEOR lead on cross-functional teams and pipeline commercialization teams, the Director represents the HEOR perspective in shaping evidence strategies across US and International markets.

This role is responsible for translating brand priorities into integrated evidence strategies that support commercialization, market access, reimbursement, and policy objectives while maintaining scientific rigor and integrity. The Director ensures HEOR plans are aligned with broader brand strategies and cross-functional evidence-generation plans.

In partnership with cross-functional leaders, the Director contributes innovative and differentiated evidence strategies, builds alignment, and gains stakeholder buy-in for evidence priorities. Leveraging deep HEOR expertise and business acumen, the Director influences indication-level decisions, prioritizes book of work within available resources, and delivers impact against brand objectives.

This is hybrid role base in Lake County, IL however, one of our other locations may be considered

Responsibilities

Accountable for developing and delivering integrated HEOR strategies for assigned indication(s); Serves as the HEOR lead on cross-functional teams, influencing key strategic decisions.; Shapes the HEOR contribution to global development, commercialization, and lifecycle strategies; Leads the HEOR evidence-generation plan, aligned with scientific, regulatory, market access, and commercial objectives.; Accountable for end-to-end delivery of the HEOR book of work, from strategy development through evidence generation, dissemination, and pull-through.; Drives lifecycle evidence and labeling strategies to support differentiation and value demonstration.; Provides strategic HEOR leadership to support market access, reimbursement, and value communication objectives.; Accountable to ensuring strong partnership with all relevant HEOR COE functions to ensure a comprehensive HEOR voice is represented in cross-functional meetings; Communicates evidence and strategic recommendations to senior internal and external stakeholders, including executives, payers, HTAs, and KOLs.; Engages senior leaders with executive presence, prioritizes the book of work within available resources, and gains stakeholder alignment.

Requirements

Advanced degree, MD, PharmD, MS in Economics, Econometrics, or (pharmaco)epidemiology; Minimum of ten years working experience with Master’s, six plus years with PhD/PharmD - Fellowship is a plus; Professional training in a health field (MD,PharmD, etc.) is a plus; Experience within pharmaceutical industry preferred.; RWE/ITC/Economic Modeling experience; Experience leading complex products and/or clinical development in support of on-market product support.; Strategic/business-minded HEOR leadership; Must perform at times in previously uncharted territory with few, if any, established guidelines or procedures. At other times, exceedingly complex governmental rules and regulations must be followed. For problems surrounded by complex rules and regulations, the Director must be able to direct compliance knowledgeably and expeditiously; Must be able to develop creative and effective solutions to inter- and intra-project priority conflicts, resource constraints and other problems which may impact project or group goals and deliverables across multiple programs; Extensive knowledge of the global regulatory, HTA and PR&A landscape, as well as understanding of other development-related functions as they relate to all phases of drug development. Experience leading complex products and/or clinical development in support of pipeline development and on-market product support; Proven leadership skills in a cross-functional global team environment. Ability to interact externally and internally to support global business strategy. Additionally, this person must be able to interact successfully with Senior Management globally (Executive staff, Area VPs, GMs etc.) and act as the HEOR project/group champion and spokesperson; High goal-orientation with the ability to see solutions rather than problems as projects encounter the inevitable ups and downs associated with new drug development or on-market product support. Must be a self- starter and have a strong desire to see projects achieve commercial success. Skills to perform the dual roles of leading a cross functional team and managing scientific personnel in clinical research; Dermatology/Immunology experience; Enterprise strategic influencer