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Located in California’s Silicon Valley, Verantos is the global leader in high-validity real-world evidence at scale. By applying artificial intelligence to the complete patient record, Verantos enables life sciences organizations to generate high-validity evidence across therapeutic areas with measured accuracy, completeness, and traceability. Credible evidence accelerates clinical development, market access, medical affairs, pharmacovigilance, and regulatory initiatives.
Verantos believes that advanced RWE requires a group of dedicated and highly-trained professionals who are specialists in the field. Our team consists of physicians, data scientists, clinical researchers and engineers with a deep knowledge of, and extensive experience in, protocol development, health system engagement, electronic health record integration, de-identification, artificial intelligence, data enrichment, study implementation and validity assessment. In addition, we have vast experience within the healthcare ecosystem, including pharma, payer, provider, and regulatory.
Position Scope and Location
You will work on advanced RWD/RWE projects with innovative biopharma companies and health systems to advance clinical research by leveraging our technology and expertise. Priorities include customer-facing and writing capabilities.
Major Responsibilities
→ Develop content required for execution and publication on projects that make significant contributions to science
Lead the development of protocols, statistical analysis plans, and requirements documents
Lead the development of abstracts and manuscripts related to studies, methods, and other efforts
→ Engage with key internal and external stakeholders
Coach and facilitate awareness of the appropriate use, timing, and implementation of epidemiologic methods and statistical techniques
Manage scientific discussions within customer and prospective customer meetings
Communicate significant scientific information to a variety of audiences
→ Execute scientifically-advanced projects
Demonstrate creative thought in applying methodological solutions that take advantage of advanced data sources and technologies
Leverage project management, product, and engineering resources to ensure timely deliverables
Collaborate with internal stakeholders to provide scientifically sound and efficient solutions to execution challenges
Required
Doctoral degree in epidemiology
At least 5 years of professional experience within a pharmaceutical firm or working with pharmaceutical firms
Excellent writing skills
Excellent verbal communication including the ability to interact with customers
Experience in the design, execution, and analysis of observational research
Creative intelligence, including a willingness to develop new methodologies that take advantage of a modern real-world evidence infrastructure using curation and data linkage
Preferred
Experience working for a data vendor, preferably a company specializing in electronic health record data
Experience working within an innovative growing startup company, including comfort with this culture
Experience performing at least one study using electronic health record unstructured data and artificial intelligence technologies
Verantos is the global leader in high-validity real-world evidence at scale. By applying artificial intelligence to the complete patient record, Verantos enables life sciences organizations to generate high-validity evidence across therapeutic areas with measured accuracy, completeness, and traceability. Credible evidence accelerates clinical development, market access, medical affairs, pharmacovigilance, and regulatory initiatives.