
Senior Director, Patient Reported Outcomes
Posted 16 hours ago

Posted 16 hours ago
This is a fully remote position, open to applicants in United States.
• Create and implement comprehensive evidence-generation strategies that highlight the humanistic value of therapies developed by BeOne Medicines.
• Provide enterprise-level leadership in Patient-Reported Outcomes (PRO) across various assets, indications, therapeutic areas, regions, and product lifecycles.
• Ensure that PRO evidence requirements are included in integrated evidence plans, medical strategies, clinical development plans, and value and access strategies.
• Consult with senior leaders and governance bodies regarding evidence priorities, investment trade-offs, methodological options, feasibility, timing, and risks.
• Supervise PRO real-world evidence, observational research, comparative effectiveness and safety studies, burden-of-illness research, patient preference studies, health economic models, indirect treatment comparisons, evidence synthesis, and value communication outputs.
• Lead intricate evidence-generation programs from inception to results dissemination and project completion.
• Manage budgets, forecasts, contracts, vendors, timelines, risks, and resource distribution.
• Ensure scientific rigor, quality controls, compliance, balanced interpretation, and independent technical reviews are maintained.
• Act as a senior PRO partner for asset teams, medical and development leadership, access teams, governance committees, and regional stakeholders.
• Translate complex scientific and economic evidence into actionable recommendations for executive, clinical, payer, regulatory, and non-technical stakeholders.
• Contribute to business development, due diligence, portfolio assessments, and evaluations of external partnerships.
• Lead or oversee strategies for publication and scientific communication.
• Represent BeOne Medicines at scientific congresses, professional associations, advisory forums, and other external engagements.
• Cultivate relationships with researchers, clinicians, payers, health economists, patient organizations, and external experts.
• Lead, mentor, and develop direct reports while providing matrix leadership to cross-functional colleagues and external teams.
• Evaluate capability and capacity needs, recommending hiring, external support, training, tools, standards, and improvements to operating models.
• An advanced degree (Masters, PhD, PharmD, MD) in health economics, outcomes research, epidemiology, biostatistics, public health, psychometrics, pharmacy, medicine, or a related quantitative or clinical field, or equivalent education and relevant experience.
• A minimum of 10 years of progressively responsible experience in PRO, real-world evidence (RWE), outcomes research, epidemiology, market access evidence, medical affairs, clinical research, or a related area.
• Significant experience in the biopharmaceutical or healthcare sectors.
• Proven success in defining and executing evidence strategies for complex assets, therapeutic areas, or portfolios in global or multi-regional settings.
• Extensive expertise in several pertinent 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 solely relying on formal authority.
• Experience in leading complex programs, managing budgets, vendors, risks, competing priorities, personnel, and matrix teams.
• Strong scientific communication skills, along with excellent written, verbal, presentation, negotiation, and stakeholder management abilities.
• Familiarity with relevant research, privacy, safety, publication, compliance, and data governance standards.
• Proficient in PC skills, including MS Office Suite and MS Teams.
• Demonstrated proficiency with productivity, collaboration, presentation, project management, and document management platforms.
• Willingness to travel approximately 25-30%, including both domestic and international travel.
• Capability to participate in meetings across various time zones and respond flexibly to urgent business needs.
• Ability to perform essential functions with or without reasonable accommodation.
• Eligibility for an annual bonus plan for non-commercial roles.
• Discretionary equity awards.
• Employee Stock Purchase Plan.
• Comprehensive medical insurance.
• Dental insurance coverage.
• Vision insurance included.
• 401(k) retirement plan.
• Flexible Spending Account (FSA) / Health Savings Account (HSA).
• Life insurance coverage.
• Paid Time Off (PTO).
• Wellness program available.
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