Director, Patient Centered Outcomes Research

Lead development and execution of evidence strategies for collecting and integrating patient experience data (PED) for assigned programs, in close collaboration with key internal and external stakeholders, aligned with clinical development timelines and health authority expectations.

Lead the development of COA measurement plans for assigned programs, including development of conceptual models, selecting, developing, and validating COA measures and endpoints for clinical and non-interventional studies (NIS). This includes input into PED/COA aspects of clinical trial protocols and statistical analysis plans (SAP), results interpretation, and dissemination.

Ensure integration of patient-experience/benefit considerations and related evidence gaps in program-level planning, as a key component of integrated evidence plans (IEP), throughout the drug research, development, and commercialization stages.

Lead design, execution, and delivery of non-interventional studies for generating regulatory-grade Patient Experience Data (PED), and COA development and validation projects.

Serve as subject matter expert on qualitative, quantitative, and mixed-methods methodologies of PED and COA measurement for assigned programs; represent PRWE in relevant cross-functional governance bodies and scientific forums.

Ensure high impact of deliverables by understanding business priorities and addressing customer needs within a matrix organizational structure.

Ensure quality, reproducibility, and compliance of all PFE deliverables with applicable regulatory guidelines and best practice [e.g., ISPOR good practice guidance, FDA PFDD guidance, China FDA guidance, and EMA PED reflection paper] and internal quality standards.

Build and maintain partnerships with academic institutions, patient advocacy groups, clinical investigators, data vendors, and CROs, aligned with program and organizational priorities.

Represent Company at scientific conferences and therapeutic area-specific meetings; contribute to peer-reviewed publications, conference presentations, and scientific communications; engage in relevant industry working groups on PFE methodology and standards.

Act as a scientific mentor and role model to less senior PFE scientists; share expertise to raise scientific standards throughout the team.

Lead PED/COA-related aspects in regulatory engagements and submissions for assigned programs, e.g., preparation of COA measure and PED dossiers.

Contribute to patient engagement activities related to program strategy or clinical studies, including patient advisory boards, panels, and councils.

Manage project-related contracting, budget, and resources; oversee vendor and partner management for assigned programs.

Master’s degree (or higher) in socio-behavioral sciences, health outcomes measurement, psychology, behavioral sciences, ethnography, psychometrics, or related field.

10+ years in patient-centered research, patient-focused drug development, or outcomes research in the Pharmaceutical/Biotech industry.

Strong understanding of clinical drug development and lifecycle management; demonstrable experience supporting key phases of a clinical program (e.g., initiation of Phase 3, regulatory filing).

Deep understanding of PFDD guidance and regulatory expectations on PFE and COA measurement, internationally (including FDA, EMA, Chinese FDA).

Demonstrable experience and knowledge of designing and implementing PED studies – applying qualitative, quantitative, and mixed-methods.

Demonstrable expertise in developing and validating COA measures.

Demonstrable experience contributing to COA/PED-related aspects in regulatory engagements and submissions.

Doctoral degree (PhD, MD) in socio-behavioral sciences or related field.

Proven ability to influence stakeholders and operate effectively in a matrixed, cross-functional environment without direct authority.

Strong conceptual, methodological, and analytical skills.

Curious, innovative, and solution-focused mentality.

Excellent scientific communication skills with ability to translate complex technical concepts into clear, actionable recommendations for diverse audiences.

Ability to work effectively in ambiguity and navigate complex stakeholder environments.

Collaborative mindset with ability to build trust across functions and with external partners.

Demonstrable ability to integrate AI tools in daily scientific work.

Experience across multiple therapeutic areas.

Familiarity with digital health technologies and wearable devices.

Experience applying novel methodologies in evidence planning and generation.

Emerging track record of scientific contributions in PFE (publications, conference presentations).

Experience with FDA/EMA COA qualification processes.

Pay Range for this position: $172,000 - 258,000

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!