Director, Global HEOR Parkinson's Disease (OUS)

The Director Health Economics & Outcomes Research (OUS) leads the development & execution of projects for onmarket 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.  The director may have 12 fulltime direct reports.      

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 consistent 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 buyin to strategies
• Accountable for endtoend 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 crossfunctional 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 Masters 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 onmarket product
• Typically 3 years of clinical development experience in the pharmaceutical industry CRO academia or other healthrelated consulting company plus having expert knowledge in a relevant therapeutic specialty
• Proven leadership skills in a crossfunctional 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 intraproject priority conflicts resource constraints and other problems which may impact project or group goals and deliverables across multiple programs.
• High goalorientation with the ability to see solutions rather than problems as projects encounter the inevitable ups and downs associated with new drug development or onmarket product support.
• Extensive knowledge of the global regulatory HTA and PR&A landscape as well as understanding of other developmentrelated 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 VPs GMs 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 shortterm incentive programs. 

• This job is eligible to participate in our longterm 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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys 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. 

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