Senior Director, Patient Reported Outcomes
B
BeOne MedicinesBiopharmaceuticals
Remote (US), Ability to participate in meetings across time zonesFull-TimeDirector
Salary$222,000.00 - $292,000.00 annually
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Job Details
- 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
- Required Skills
- MS Office
Requirements
- Hold an advanced degree 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.
- Have 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.
- Bring substantial biopharmaceutical or healthcare-sector experience.
- Demonstrate success defining and executing evidence strategies for complex assets, therapeutic areas, or portfolios in a global or multi-regional environment.
- Have deep expertise in several relevant methods, including observational study design, causal inference, comparative effectiveness, economic modeling, indirect treatment comparisons, evidence synthesis, PRO/COA methods, or patient preference research.
- Demonstrate ability to influence senior leaders, governance bodies, and cross-functional teams without relying solely on formal authority.
- Show leadership of complex programs, budgets, vendors, risks, competing priorities, people, and matrix teams.
- Have a strong scientific communication record and written, verbal, presentation, negotiation, and stakeholder-management skills.
- Have working knowledge of applicable research, privacy, safety, publication, compliance, and data-governance expectations.
- Be able to travel approximately 25–30%, including domestic and international travel, and participate in meetings across time zones.
- PC skills, including MS Office Suite and MS Teams; proficiency with productivity, collaboration, presentation, project-management, and document-management platforms.
Responsibilities
- Own and provide senior leadership for global or regional PRO strategy across assigned assets, programs, therapeutic areas, or portfolios.
- Shape integrated evidence plans by identifying, prioritizing, and revisiting evidence gaps with cross-functional leadership.
- Advise senior leaders and governance bodies on evidence priorities, investment trade-offs, methodological options, feasibility, timing, and risk.
- Provide scientific oversight for PRO real-world evidence, observational research, comparative effectiveness and safety research, patient preference research, and value communication deliverables.
- Lead complex evidence-generation programs from concept through results dissemination and project closure.
- Oversee project budgets, forecasts, contracts, vendor performance, timelines, risks, and resource allocation.
- Translate complex scientific and economic evidence into recommendations for executive, clinical, payer, regulatory, and nontechnical audiences.
- Lead or oversee publication and scientific communication strategies for assigned PRO programs.
- Lead, coach, and develop direct reports and provide matrix leadership to cross-functional colleagues and external research teams.
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