Advarra · 9 hours ago
Clinical Strategy & Analytics Scientist
Advarra is a leader in clinical research and health advancement, dedicated to connecting patients, sites, sponsors, and CROs. The Clinical Strategy & Analytics Scientist will leverage clinical development expertise and advanced analytics to generate actionable insights that optimize protocol design and operational strategies for clinical trials.
Pharmaceutical
Responsibilities
Serve as the scientific lead for interpreting clinical research dataset outputs, including eligibility, enrollment modeling, site capabilities and performance, and operational risk indicators and key performance metrics
Develop, refine, and review analytical workflows that support protocol optimization, scenario modeling, trend analyses, and study start up forecasting
Identify data trends, evaluate signals and translate insights into clear narratives, hypotheses, and decision-ready strategic insights for sponsors and stakeholders
Partner with product and data science teams to validate and refine analytic models, dashboards, and insight templates
Influence product design by articulating scientific requirements needed to ensure models, dashboards, and insights align with trial design realities
Interpret protocol elements to assess burden, complexity, and downstream operational challenges
Contribute to scientific frameworks and best practices that advance insights-driven protocol design. across Advarra’s product ecosystem
Serve as a scientific expert in sponsor-facing engagements, including insight readouts, protocol optimization reviews, and feasibility deep dives
Lead presentation of scientific findings and engage in detailed discussions with clinical development leaders, operational teams, and cross-functional sponsor stakeholders
Develop and refine customer-facing deliverables, including protocol optimization reports, scenario analyses, feasibility briefs, and operational insight summaries
Represent clinical science for strategic customers and external collaborations, providing scientific guidance and supporting follow-up discussions as needed
Act as the clinical science liaison to product, engineering, and data science teams, advocating for scientific accuracy, operational relevance, and model interpretability across the roadmap
Support the development of scalable methodologies, templates, and playbooks for insights delivery, data interpretation, and protocol evaluation
Qualification
Required
Advanced scientific or healthcare degree (PhD, PharmD, MS, MPH, RN, or equivalent experience)
7+ years of experience in clinical science, clinical development, or clinical operations within biotech, pharma, or CRO environments
Experience leading scientific and operational aspects of clinical trials including protocol development, study startup, conduct, and data interpretation
Demonstrated fluency and experience in analytics and data interpretation
Experience working with data scientists and understanding structured clinical operations datasets
Preferred
Experience with scenario analysis, enrollment modeling, feasibility assessment, or site selection analytics
Familiarity with trial planning technologies, data visualization platforms, and operational intelligence tools
Understanding of real-world data sources, eligibility logic, trial registries, and diversity planning in clinical research
Experience reviewing protocol deviations, data trends, and operational quality indicators
Background supporting global clinical studies, including protocol versioning, CRF design alignment, DMC or adjudication committee interactions, or clinical narrative review
Comfortable working in a fast-moving environment focused on new product development and client delivery
Benefits
Health coverage
Paid holidays
Variable bonus
Company
Advarra
Advarra leverages exceptional client service, innovative technology, enhanced regulatory expertise and global research compliance services.
Funding
Current Stage
Late StageTotal Funding
unknown2022-06-10Acquired
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