Associate Director Real World Value & Evidence

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Job Function:
Market Access

Job Sub Function:
Health Economics Outcomes Research

Job Category:
Professional

All Job Posting Locations:
Titusville, New Jersey, United States of America

Job Description:
Job Description

The Associate Director, Real-World Evidence is responsible for leading real-world evidence activities in support of CAPLYTA and the assigned portfolio.

This individual connects evidence-generation strategy with rigorous RWE study design, operational execution, data interpretation, and scientific dissemination.

The Associate Director collaborates with internal and external clinical, RWE, epidemiology, analytics, safety, operations, and medical affairs experts to generate high-quality real-world evidence.

The role is accountable for the quality of RWE study design, execution, interpretation, publication, and related models/tools developed for internal and external stakeholders.

This role also incorporates selected Clinical Project Scientist responsibilities where they strengthen RWE execution, including oversight of non-interventional research activities, post-marketing research programs, protocol development, study close-out activities, operational issue resolution, budget/contract coordination, and compliant cross-functional collaboration.

Key Responsibilities

• Lead the design, implementation, and direct management of real-world evidence studies, non-interventional research activities, post-marketing research programs, and RWE-related models/tools from concept through publication.

• Formulate key RWE research questions, recommend fit-for-purpose methods, and ensure scientific rigor across retrospective and prospective data analyses, epidemiology, patient-reported outcomes, health services research, and other real-world data approaches.

• Develop and execute analytic plans using relevant healthcare data sources, including claims databases, electronic health records, registries, patient-level longitudinal datasets, and other real-world data sources, where appropriate.

• Provide active scientific and operational input to protocol development, RWE study design, amendments, study reports, clinical study reports, ...