About the job
Join AbbVie’s Aesthetics and Plastics & Regenerative Medicine (PRM) Health Economics & Outcomes Research (HEOR) Strategy team, a critical part of our Patient Centered Outcomes Research (PCOR) Center of Excellence. As the Associate Director for Aesthetics & PRM HEOR Strategy, you will report directly to the Director, spearheading the development and execution of strategic projects for both marketed and pipeline Aesthetics assets. You will be instrumental in designing and implementing patient experience data (PED) strategies, focusing on patient-reported outcomes (PRO) development, regulatory communications, and prospective observational studies to support product approval, differentiation, and market access. Acting as a subject matter expert in PED and patient-centered measurement strategies, you will collaborate with cross-functional teams including Clinical Development, Medical Affairs, Regulatory, and Commercial to elevate PED standards and best practices, fostering a patient-centric culture throughout AbbVie.
Key Responsibilities:
- Formulate and execute HEOR and Patient Experience Data (PED) strategies to facilitate product approval, differentiation, and market access for Aesthetics assets.
- Lead comprehensive global PED and Clinical Outcomes Assessment (COA) research, including PRO development and innovative patient-relevant measures.
- Direct the planning and execution of prospective observational surveys and electronic medical records to enhance AbbVie Aesthetic assets based on real-world effectiveness.
- Oversee study design, execution, and dissemination of findings, ensuring scientific rigor and timely delivery in line with asset strategies.
- Serve as a subject matter expert, promoting cross-functional collaboration with Clinical Development, Regulatory, Commercial, and other stakeholders to integrate PED and HEOR plans within the broader evidence strategy.
- Drive regulatory and reimbursement strategies concerning PED, contributing to submissions, addressing patient-focused endpoints, and engaging in key negotiations to optimize registration, labeling, and access decisions.
- Develop and implement best practices and educational resources to enhance the integration of patient voice and PED standards across AbbVie.
- Uphold high standards for scientific quality, including proposal, protocol, analysis development, and effective communication of research in both internal and external forums.
- Lead strategic scientific communication efforts, including the development of manuscripts, abstracts, and conference presentations.
- Stay updated on methodological advancements, regulatory requirements, and industry trends to ensure innovative and compliant PED/COA strategies.

