Physician Researcher, Study Design, Registry

Verily

Physician Researcher leading study design and registry development at Verily Health. Engaging with external stakeholders and ensuring compliance with scientific standards in health solutions.

Posted 7/18/2026full-timeDallas • California, Massachusetts, North Carolina, Texas • 🇺🇸 United StatesMid-LevelSenior💰 $122,000 - $183,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading the design and execution of registries and real-world evidence studies, with a strong foundation in epidemiological methods and biostatistics. Capable of fostering strategic partnerships and ensuring compliance with regulatory standards in clinical research.

Highest-signal resume keywords

M.D. Or D.O.Clinical Development ExperienceEpidemiological MethodsReal-World Evidence StudiesGCP Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research DesignBiostatistics FundamentalsObservational Research ProtocolsRegulatory ComplianceReal-World Data Analysis

Soft Skills

Excellent Communication SkillsLeadershipCollaboration

Certifications & Qualifications

Active Medical Licensure

Industry Keywords

Pharmaceutical IndustryBiotechCROClinical AffairsResearch Partnerships

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead the design of registries, observational studies, and pragmatic/real-world evidence (RWE) studies
Serve as the primary clinical point of contact for external customers, investigators, sites, and partner organizations
Partner with Clinical Operations, Biostatistics, Epidemiology, and Regulatory Affairs to ensure protocols meet scientific, regulatory, and operational standards
Identify, cultivate, and lead strategic research partnerships with academic medical centers, health systems, professional societies, and external research networks

Requirements

What you’ll need

M.D. or D.O. (or international equivalent) with active or eligible medical licensure
3–5 years of pharmaceutical, biotech, or CRO industry experience in clinical development, medical affairs, or real-world evidence
Strong understanding of epidemiological methods, biostatistics fundamentals, and real-world data sources
Working knowledge of GCP and regulatory requirements for observational research
Excellent written/verbal communication skills across scientific and non-scientific audiences

Benefits

Comp & perks

flexible work arrangements
wellness programs