Senior Director, Real World Evidence
New
Based in the United StatesFull-TimeDirector
Salary280,000 - 308,000 USD per year
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Job Details
- Experience
- 13+ years
Requirements
- Advanced degree (PhD, MD, PharmD, MPH, MSc, or equivalent) in epidemiology, biostatistics, health economics, health services research, or a related field.
- Minimum of 13+ years of experience in pharmaceutical, biotechnology, or HEOR consulting environments focused on real-world evidence.
- At least 10 years of leadership experience managing teams and large-scale RWE or HEOR programs.
- Demonstrated expertise in designing and executing observational studies using large real-world datasets across multiple phases of the product lifecycle.
- Proven experience leading center-of-excellence or enterprise-level RWE functions.
- Strong background in building external data partnerships and managing vendor ecosystems.
- Experience supporting regulatory submissions, HTA dossiers, and market access evidence requirements.
- Deep methodological expertise in epidemiology, outcomes research, and quantitative analytics.
- Strong leadership, communication, and stakeholder management skills.
Responsibilities
- Lead the end-to-end Real-World Evidence (RWE) program, translating enterprise evidence priorities into high-quality observational study designs and deliverables.
- Provide strategic leadership, mentorship, and career development for a team of RWE Scientists.
- Oversee design and execution of studies including burden-of-illness, patient journey, drug utilization, comparative effectiveness, external control arms, and HTA-supportive analyses.
- Establish methodological standards, statistical frameworks, protocol templates, and quality benchmarks for all RWE activities.
- Lead the development and execution of registry-based studies and large healthcare database analyses across the product lifecycle.
- Partner with IT and Commercial teams to build scalable real-world data infrastructure and analytics capabilities.
- Lead publication strategy and represent the organization at scientific conferences.
- Ensure compliance with applicable regulatory, ethical, and data governance standards.
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