Senior Director, Patient Reported Outcomes

Job not on LinkedIn

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $222k - $292k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 0%

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BeOne Medicines

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2010

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 Description

• 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

• 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

• 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