Lilly
healthcare
Director,RWE,CMH
“Director, RWE, CMH at Lilly. Skills: Real-World Evidence strategy, evidence generation, study design, epidemiologic methods, statistical methods, cross-functional leadership, communication. driving the Real-World Evidence strategy and execution within Medical Affairs. ensure that robust, high-quality evidence is generated and communicated”
What You'll Achieve.
ensure that robust, high-quality evidence is generated and communicated to inform clinical practice, regulatory/payer decisions, and healthcare policy; address critical data gaps across the product lifecycle; position the company as a scientific leader and trusted partner in improving patient outcomes
Industry & Context.
Prioritize and address evidence gaps related to disease burden, treatment patterns, patient outcomes, safety, and comparative effectiveness.
hybrid role – onsite presence at our Toronto office will be 10 days or more per month (or at least 50% of the time)
What They're Looking For.
Must Have
Advanced degree in epidemiology, health economics, outcomes research, biostatistics, medicine, or related discipline (PhD, MD, PharmD, or MPH with RWE experience), 8+ years’ experience in pharmaceuticaliotech industry, CRO, or academia with direct RWE/observational research leadership, Demonstrated expertise in study design, epidemiologic/statistical methods, and working with RWD assets, understanding of payer/HTA requirements, regulatory frameworks, and GPP/GCP compliance, Proven track record of peer-reviewed publications, congress presentations, and cross-functional leadership, Excellent communication ability to influence internal and external stakeholders at senior levels, Experience managing vendors, RWE budgets, and complex project portfolios
What You'll Do.
driving the Real-World Evidence strategy and execution within Medical Affairs
high-quality evidence is generated and communicated
address critical data gaps across the product lifecycle
lead the design development
and oversight of observational studies
external control arms
and patient-reported outcome research
manage vendor/CRO partnerships for study execution
oversee due diligence and utilization of real-world data (RWD) assets
serve as the Medical Affairs RWE point of contact for internal stakeholders
training teams on RWE interpretation and application
drive dissemination of RWE through publications
congress presentations
and educational activities
provide RWE insights to inform medical education
and health policy discussions
provide mentorship to junior RWE scientists and medical team members
champion innovation in data science
and digital RWE solutions
contribute to enterprise-wide RWE governance
and capability building
How You'll Work.
Team & Collaboration
Collaborate and align with Sr. Medical Director/Director/Medical Advisor to develop the integrated evidence generation strategy; Partner closely with HEOR, Market Access, Regulatory, Clinical Development, Pharmacovigilance, and Commercial Insights; Serve as the Medical Affairs RWE point of contact for internal stakeholders; Support Sr. Medical Director/Director/Medical Advisor in engagements and interactions with KOLs, academic collaborators, patient registries, and external data consortia
Communication Scope
Excellent communication ability to influence internal and external stakeholders at senior levels; drive dissemination of RWE through publications, congress presentations, dossiers, and educational activities; Provide RWE insights to inform medical education, payer submissions, label expansion, and health policy discussions
Process & Methodology
managing complex project portfolios
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