Senior Director, Patient Reported Outcomes

BeOne Medicines

. Develop and execute integrated evidence-generation strategies demonstrating the humanistic value of BeOne Medicines therapies .

Posted 10/5/2026full-timeRemote • United StatesSenior💰 $222,000 - $292,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced expertise in developing and executing evidence-generation strategies, particularly in health economics and outcomes research. Proven ability to lead complex programs and influence stakeholders across various levels while ensuring scientific rigor and compliance.

Highest-signal resume keywords

Advanced Degree In Health Economics10+ Years In PRO And RWEExpertise In Observational Study DesignStrong Scientific Communication SkillsExperience Leading Complex Programs

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Health EconomicsOutcomes ResearchEpidemiologyBiostatisticsComparative EffectivenessEconomic ModelingPatient Preference ResearchEvidence SynthesisPRO/COA MethodsData Analysis

Soft Skills

Influencing Senior LeadersStakeholder ManagementNegotiationPresentation SkillsTeam Leadership

Tools & Technologies

MS Office SuiteMS TeamsProject Management PlatformsDocument Management PlatformsCollaboration Tools

Industry Keywords

Biopharmaceutical ExperienceHealthcare Sector ExperienceReal-World EvidenceMarket Access EvidenceClinical ResearchScientific CommunicationComplianceData GovernanceBudget ManagementCross-Functional Leadership

About the role

Key responsibilities & impact

Develop and execute integrated evidence-generation strategies demonstrating the humanistic value of BeOne Medicines therapies
Provide enterprise-level PRO leadership across assets, indications, therapeutic areas, regions, and product lifecycles
Ensure PRO evidence needs are represented in integrated evidence plans, medical strategies, clinical development plans, and value and access strategies
Advise senior leaders and governance bodies on evidence priorities, investment trade-offs, methodological options, feasibility, timing, and risk
Oversee PRO real-world evidence, observational research, comparative effectiveness and safety research, burden-of-illness studies, patient preference research, health economic models, indirect treatment comparisons, evidence syntheses, and value communication deliverables
Lead complex evidence-generation programs from concept through results dissemination and project closure
Oversee budgets, forecasts, contracts, vendors, timelines, risks, and resource allocation
Ensure scientific rigor, quality controls, compliance, balanced interpretation, and independent technical review
Serve as senior PRO partner to asset teams, medical and development leadership, access teams, governance committees, and regional stakeholders
Translate complex scientific and economic evidence into recommendations for executive, clinical, payer, regulatory, and nontechnical audiences
Contribute to business development, due diligence, portfolio assessment, and external partnership evaluations
Lead or oversee publication and scientific communication strategies
Represent BeOne Medicines at scientific congresses, professional associations, advisory forums, and external engagements
Build relationships with researchers, clinicians, payers, health economists, patient organizations, and external experts
Lead, coach, and develop direct reports and provide matrix leadership to cross-functional colleagues and external teams
Assess capability and capacity needs and recommend hiring, external support, training, tools, standards, and operating-model improvements

Requirements

What you’ll need

Advanced degree (Masters, PhD, PharmD, MD) in health economics, outcomes research, epidemiology, biostatistics, public health, psychometrics, pharmacy, medicine, or a related quantitative or clinical discipline, or equivalent education and relevant experience
10 or more years of progressively responsible experience in PRO, RWE, outcomes research, epidemiology, market access evidence, medical affairs, clinical research, or a related field
Substantial biopharmaceutical or healthcare-sector experience
Success defining and executing evidence strategies for complex assets, therapeutic areas, or portfolios in a global or multi-regional environment
Deep expertise in several relevant methods, including observational study design, causal inference, comparative effectiveness, economic modeling, indirect treatment comparisons, evidence synthesis, PRO/COA methods, patient preference research, or analysis of claims, electronic health records, registries, or clinical-trial data
Ability to influence senior leaders, governance bodies, and cross-functional teams without relying solely on formal authority
Experience leading complex programs, budgets, vendors, risks, competing priorities, people, and matrix teams
Strong scientific communication record and excellent written, verbal, presentation, negotiation, and stakeholder-management skills
Working knowledge of applicable research, privacy, safety, publication, compliance, and data-governance expectations
PC skills, including MS Office Suite and MS Teams
Proficiency with productivity, collaboration, presentation, project-management, and document-management platforms
Ability to travel approximately 25–30%, including domestic and international travel
Ability to participate in meetings across time zones and respond flexibly to critical business needs
Ability to perform essential functions with or without reasonable accommodation

Benefits

Comp & perks

Annual bonus plan eligibility for non-commercial roles
Discretionary equity awards
Employee Stock Purchase Plan
Medical insurance
Dental insurance
Vision insurance
401(k)
FSA/HSA
Life Insurance
Paid Time Off
Wellness program