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About the Role

The International RWE Lead will serve as the primary interface for the international real-world evidence (RWE) community, linking area and affiliate stakeholders to the Medical Affairs + Health Impact (MHI) RWE Center of Excellence (CoE), and cross-functional research functions. This role will enable the generation of fit-for-purpose RWE via use of optimal RWD and methodologies across international affiliates and act as a crucial nexus across AbbVie's RWE capabilities.

Responsibilities

Serve as the RWE subject matter expert within the assigned region and/or therapeutic areas, championing the understanding and use of primary and secondary RWD and supporting affiliates/areas in the translation of evidence gaps to robust and tangible study design through methodological input.
Work with the Value and Evidence RWE pillars and cross-functional research functions to coordinate optimal expertise based on specific International Area & Affiliate research needs.
Contribute to building Global-International and affiliate-area RWE networks, highlighting available expertise & resources and delivering RWD/E input and training.
Co-lead the Asset RWE Community in partnership with International Medical and Market Access including defining the specific needs, format and membership for each asset.
Support evidence planning to focus on optimal real world study design to meet strategic cross-functional needs.
In collaboration with Global RWE Innovative Real-World Data and Policy, stay current with evolving RWE guidelines, innovations, emerging trends and best practices.
Represent AbbVie on relevant external consortia and partner with local stakeholders to drive innovative use of RWD.
Serve as a member of the Area Review Committee (ARC), Area Evidence Teams and priority Local Evidence Teams, as needed, providing input into International evidence plans.
Engage with external vendors/data owners to identify opportunities for smart evidence generation.
Represent AbbVie at external and internal International RWE meetings, as needed.
Support evolution of International knowledge and use of RWD sources, in partnership with the V&E RWE CoE’s and cross-functional research functions.
Represent International RWE in internal RWD/E and evidence generation workstreams, as needed.
Actively engage with the broader International and US RWE lead community to share ideas, learnings and best practices to evolve RWE customer excellence.

Requirements

Advanced degree in public health, health economics, outcomes research, epidemiology, biostats, or another relevant field.
Minimum of 8-10 years hands-on experience in international RWE, outcomes research, etc. within the pharmaceutical, academia, or consultancy sectors to support market access, medical and commercial evidence needs.
Demonstrated experience with study/protocol design to meet strategic needs using a range of RWD sources.
Deep understanding of OUS RWD/E landscape in at least 1 region (Europe, JAPAC, Canada, LATAM).
Analytics experience desirable but not essential.
Understands pharma asset strategy and has demonstrated experience in area or global integrated evidence planning and subsequent planning of RWE studies/initiatives.
Strong influencing without authority skills.
Demonstrated experience at coaching study teams or decision makers (expert and non-expert) through RWE study design decisions drawing upon scientific, strategic and practical needs.
Individual must have demonstrated ability to work successfully in a cross-matrix setting.
Skilled in consultant, team member and team lead working styles and able to flex working style to meet the specific project needs.
Fluent at conveying complex information and context to expert and non-expert audiences in a clear and relevant manner.
Compelling, adaptable communicator to small and large audiences across functions and levels of seniority.
Ability to develop plans and self-manage timelines, resources, and deliverables effectively.
Must be comfortable to perform in previously uncharted territory with few, if any, established use cases, guidelines or processes.
Flexibility to adjust based on changing circumstances and openness to new ideas and continuous learning.
Oncology (heme, solid tumors), immunology or neurology indications strongly desired.
Must be fluent in English.
Additional languages in relevant geographical region are desirable but not essential.

Skills

RWE
Real-world data (RWD)
Methodological input
Study design
Integrated evidence planning
Influencing
Consultancy
Communication
Project management

Experience Level

8-10 years

Education Level

Advanced degree

Salary/Compensations

USD 124500 - USD 236500 - yearly

Benefits

Paid time off (vacation, holidays, sick)
Medical/dental/vision insurance
401(k)
Long-term incentive programs

About the Company

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.

Equal Opportunity

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