Director, HEOR Strategy Eyecare, International Launch Lead

The Director Health Economics & Outcomes Research (HEOR) leads the strategic development & execution of high-quality evidence for an enterprise-critical gene therapy in retina diseases. He or she directly contributes to the launch evidence required for JCA and HTA and serves as the brand/asset leader representing HEOR on cross functional asset/brand teams   ensuring HTA/payer evidence requirements are reflected in the overall asset strategy. He or she may be accountable for  more than one asset and/or   indication and oversees evidence alignment across key international markets.   

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. These activities include but are not limited to: multi-stakeholder unmet need evidence cost effectiveness and economic modeling comparative effectiveness analyses real world evidence patient reported outcomes and working with external experts to substantiate the case for gene therapy policy change
• 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 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 :

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 global launch
• 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 HEOR. 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 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 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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Work :

No

Employment Type :

Full-time