Director, HEOR Strategy Solid Tumors
Allergan, Greenlawn, NY, United States
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 at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description The Director, Health Economics & Outcomes Research (HEOR) leads the development & execution of projects for on‑market and/or pipeline development assets, who is the brand/asset leader representing HEOR on cross‑functional asset/brand teams and in the pipeline commercialization teams. He or she is accountable for HEOR strategies and execution for at least one asset and/or at least one indication for US or international.
Responsibilities
Oversees the design and conduct of projects and effectively communicates the findings and strategic impact of findings to internal and external audiences
Provides product leadership to HEOR strategic direction for consistency with business goals established in conjunction with the appropriate cross‑functional partners
Ensures project plan integrates and aligns with the product strategic plans from matrix teams as well as commercial interests. Provides updates on execution of plans to product as well as functional management, owns, then shares project execution decisions. In the development of product strategic plans he/she liaises with other members of the product team to generate innovative ideas and create buy‑in to strategies
Accountable for end‑to‑end delivery of HEOR book of work under their remit, from strategy development to content pull‑through
Accountable to ensuring strong partnership with all relevant HEOR COE functions to ensure a comprehensive HEOR voice is represented in cross‑functional meetings
Executive presence and ability to engage with senior leaders in a cross‑functional setting
Qualifications
Advanced degree in health economics or related discipline
Minimum of seven years working experience with Master’s, five year with PhD (can include fellowship experience). Professional training in a health field (MD, PharmD, etc.) is a plus
Preferred: PhD in Economics, Econometrics, or (pharmaco)epidemiology or any other related field with 3 years of relevant experience. Clinical research experience strongly recommended; within pharmaceutical industry preferred. Experience leading complex products and/or clinical development in support of pipeline development and on‑market product
Typically 3+ years of clinical development experience in the pharmaceutical industry, CRO, academia or other health‑related consulting company plus having expert knowledge in a relevant therapeutic specialty
Proven leadership skills in a cross‑functional global team environment. Ability to interact externally and internally to support global business strategy
The Director 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
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
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
Skills to perform the dual roles of leading a cross functional team and managing scientific personnel in clinical research. Must be able to interact successfully with Senior Management globally (Executive staff, Area VP, GM etc.) and act as the HEOR project/group champion and spokesperson. Additionally, must be a self‑starter and have a strong desire to see projects achieve commercial success
Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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 time of 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 the future
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 short‑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 employee remains in the Company's sole and absolute discretion 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, visit https://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
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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.
Job Description The Director, Health Economics & Outcomes Research (HEOR) leads the development & execution of projects for on‑market and/or pipeline development assets, who is the brand/asset leader representing HEOR on cross‑functional asset/brand teams and in the pipeline commercialization teams. He or she is accountable for HEOR strategies and execution for at least one asset and/or at least one indication for US or international.
Responsibilities
Oversees the design and conduct of projects and effectively communicates the findings and strategic impact of findings to internal and external audiences
Provides product leadership to HEOR strategic direction for consistency with business goals established in conjunction with the appropriate cross‑functional partners
Ensures project plan integrates and aligns with the product strategic plans from matrix teams as well as commercial interests. Provides updates on execution of plans to product as well as functional management, owns, then shares project execution decisions. In the development of product strategic plans he/she liaises with other members of the product team to generate innovative ideas and create buy‑in to strategies
Accountable for end‑to‑end delivery of HEOR book of work under their remit, from strategy development to content pull‑through
Accountable to ensuring strong partnership with all relevant HEOR COE functions to ensure a comprehensive HEOR voice is represented in cross‑functional meetings
Executive presence and ability to engage with senior leaders in a cross‑functional setting
Qualifications
Advanced degree in health economics or related discipline
Minimum of seven years working experience with Master’s, five year with PhD (can include fellowship experience). Professional training in a health field (MD, PharmD, etc.) is a plus
Preferred: PhD in Economics, Econometrics, or (pharmaco)epidemiology or any other related field with 3 years of relevant experience. Clinical research experience strongly recommended; within pharmaceutical industry preferred. Experience leading complex products and/or clinical development in support of pipeline development and on‑market product
Typically 3+ years of clinical development experience in the pharmaceutical industry, CRO, academia or other health‑related consulting company plus having expert knowledge in a relevant therapeutic specialty
Proven leadership skills in a cross‑functional global team environment. Ability to interact externally and internally to support global business strategy
The Director 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
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
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
Skills to perform the dual roles of leading a cross functional team and managing scientific personnel in clinical research. Must be able to interact successfully with Senior Management globally (Executive staff, Area VP, GM etc.) and act as the HEOR project/group champion and spokesperson. Additionally, must be a self‑starter and have a strong desire to see projects achieve commercial success
Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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 time of 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 the future
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 short‑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 employee remains in the Company's sole and absolute discretion 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, visit https://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
#J-18808-Ljbffr