Director, Physician Researcher – Evidence Generation & Registries
$291,000–$328,000 year
On-siteBoston, Massachusetts, United States or Dallas, Texas, United States
Job Summary
Lead the design of registries, observational studies, and pragmatic real-world evidence studies, including protocol development, endpoint selection, statistical analysis planning, and data collection instruments. Shape Verily's evidence generation strategy and standards across clinical programs, digital health products, and care delivery models. Serve as the primary clinical point of contact for external customers, investigators, and partners, presenting study design rationale and representing Verily at conferences and advisory boards. Oversee the responsible use of AI-enabled research tools, evaluating outputs for accuracy, bias, and clinical validity against predefined quality standards. Partner with biostatistics, epidemiology, data science, product, regulatory, and commercial teams, and mentor junior clinical and research staff.
Required Qualifications
- MD, DO, or equivalent doctoral-level degree with active or eligible medical licensure
- 10+ years of experience in evidence generation, real-world evidence, clinical outcomes research, clinical development, or medical affairs in a pharmaceutical, biotech, healthcare technology, or CRO environment
- Demonstrated experience designing and leading observational studies, registries, or pragmatic clinical trials using real-world data sources (claims, EHR, patient-reported outcomes)
- Experience in a customer- or partner-facing role, leading scientific discussions with external investigators, KOLs, and institutional stakeholders
- Experience evaluating AI-enabled tools in a clinical research, registry, or real-world data context
- Qualified applicants must not require employer sponsored work authorization now or in the future for employment in the United States
Desired Qualifications
- Advanced degree (MPH, MSCE, or similar) in epidemiology, clinical research, or public health
- Authorship of peer-reviewed publications involving observational or registry data, and experience presenting at national conferences
- Working knowledge of GCP, FDA real-world evidence guidance, ISPOR/ISPE good practice standards, IRB protocol development, and data privacy requirements (HIPAA, GDPR)
- Experience mentoring or managing clinical, scientific, research, or analytics talent
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