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Associate Director, HEOR Strategy - Aesthetics

Job in Greenlawn, Suffolk County, New York, 11740, USA
Listing for: Allergan
Full Time position
Listed on 2026-02-05
Job specializations:
  • Healthcare
    Healthcare Administration, Healthcare Management
Job Description & How to Apply Below
Location: Greenlawn

Company Description

Abb Vie’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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok.

Job Description

Abb Vie’s Aesthetics and Plastics & Regenerative Medicine (PRM) Health Economics & Outcomes Research (HEOR) Strategy team is part of the Patient Centered Outcomes Research (PCOR) Center of Excellence. The Associate Director in the Aesthetics & PRM HEOR-Strategy will report to the Director and lead the development and execution of strategically aligned projects for both marketed and pipeline Aesthetics assets. The AD will design and implement patient experience data (PED) strategies - including PRO development, regulatory communications, and prospective observational studies - to support product approval, differentiation, and access.

The AD will act as a subject matter expert on PED and patient-centered measurement strategies, collaborating cross-functionally (e.g., with Clinical Development, Medical Affairs, Regulatory, and Commercial teams) advancing the adoption of PED standards and best practices to foster a patient-centric culture across Abb Vie.

Responsibilities:

  • Develop and execute HEOR and Patient Experience Data (PED) strategies to enable product approval, differentiation, and market access for Aesthetics assets
  • Lead the planning, management, and execution of global PED and Clinical Outcomes Assessment (COA) research, including PRO development, innovative patient-relevant measure
  • Lead the planning, management, and execution of prospective observational surveys and electronic medical records to differentiate Abb Vie Aesthetic assets based on real-world effectiveness, creation, and integration into clinical programs
  • Oversee study design, execution, and dissemination of findings, ensuring scientific rigor and timely delivery aligned with asset strategies
  • Act as a subject matter expert, facilitating cross-functional collaboration (Clinical Development, Regulatory, Commercial, and other stakeholders) to align and integrate PED and HEOR plans within broader evidence strategy
  • Drive regulatory and reimbursement strategies relating to PED, contributing to submissions, addressing patient-focused endpoints, and participating in key negotiations to optimize registration, labeling, and access decisions
  • Develop and implement best practices and educational resources to advance the integration of patient voice and PED standards across Abb Vie
  • Maintain high standards for scientific quality, including proposal, protocol, analysis development, and effective communication of research in internal and external forums
  • Lead strategic scientific communication, including manuscript, abstract, and conference presentation development
  • Stay current on methodological advancements, regulatory requirements, and industry trends to ensure innovative and compliant PED/COA strategies
    • Qualifications
    • Advanced degree in Psychology, Epidemiology, Statistics, Public Health, Health Economics and Outcomes Research (HEOR) or related discipline (MS, MPH, Pharm

      D, PhD) preferred
    • Minimum of 5 years of experience required, with relevant pharmaceutical industry or consulting experience in patient experience data research; clinical outcome assessment / patient reported outcome development, psychometric validation, and implementation; and medical product development and trial design
    • Demonstrated ability in evaluation & development of PED from conceptualization through negotiations by global authorities
    • Experience in preparing regulatory & HTA submissions
    • Excellent interpersonal skills with an ability to leverage deep expertise to understand, respond and influence effectively across multiple internal and external customers
    • Demonstrated ability to manage multiple priorities in rapidly changing environment
    • Excellent…
    Position Requirements
    10+ Years work experience
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