Director, US Real-World Evidence & Health Outcomes -Multiple Myeloma
HybridPhiladelphia, Pennsylvania, United States or Durham, North Carolina, United States
Job Summary
Develop evidence generation plans and design multiple real-world evidence and health outcomes studies aligned with US medical, payer, and access needs. Lead day-to-day execution of assigned studies, including cost-effectiveness analyses and treatment patterns, in partnership with internal functions and external vendors. Manage cross-functional stakeholder meetings to align on evidence gaps and priorities, while drafting protocols, statistical analysis plans, and manuscripts to ensure high scientific quality. Provide RWE input to internal decision-making during product development and commercialization planning, incorporating field-based payer insights into value communication strategies. Manage vendor contracts, track budgets, and escalate risks proactively to ensure timely delivery of high-quality evidence supporting product positioning.
Required Qualifications
- Master's degree or PhD in health economics and outcomes research, epidemiology, public health, biostatistics, or related discipline
- 3+ years' experience within the pharmaceutical industry
- US Oncology experience
- Designing a publication plan
- Having a presence of RWE/HO research studies at major clinical congresses
- Experience managing multiple projects simultaneously
- Expertise in RWE and economic evaluation study designs/methods
- Evidence of publications and/or contributing to study concept sheets and protocols
- Reviewing/authoring key sections of statistical analysis plans and study reports
- Ensuring publication/disclosure readiness in accordance with internal SOPs and external requirements
- Strong communication and presentation skills
- Proven ability to prioritize, pivot, and manage multiple projects simultaneously in a matrix environment
Desired Qualifications
- Demonstrated success developing and executing health outcomes research plans and delivering high-quality data generation outputs
- Oncology experience (US or global), including familiarity with evolving standards of care, evidence requirements, and stakeholder needs across disease areas
- Masters + ~4–6 years or PhD with 2–4+ years of experience within the pharmaceutical industry and/or managed care, hospital, academic, or healthcare consulting environment
- Experience collaborating with field-facing teams (e.g., Field Based Payer Medical, Field Medical) and/or Market Access partners
- Experience managing real-world data sources and vendors (e.g., claims, EHR, registries)
- Translating findings into actionable insights and value messages
- Demonstrated ability to influence without authority in a matrix environment
- Strategic execution experience, demonstrated by translating evidence strategy into workplans (milestones, timelines, resourcing) and delivering outputs across 1–2 concurrent asset workstreams
- Demonstrated project and vendor management experience, including defining scope and success criteria, tracking budgets/timelines, proactively identifying risks/issues, and implementing mitigation plans through change control
- Experience contributing to congress strategy and publication planning (abstracts, posters, manuscripts)
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