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Sr. Quantitative Scientist – Commercial-Facing

Sr. Quantitative Scientist – Commercial-Facing

CompanyVerana Health
LocationKnoxville, TN, USA, San Francisco, CA, USA, New York, NY, USA
Salary$150000 – $175000
TypeFull-Time
DegreesMaster’s, PhD
Experience LevelSenior

Requirements

  • Master’s or doctorate in a quantitative discipline (e.g., biostatistics, epidemiology, health economics, etc.) or equivalent practical experience
  • 5+ years of hands-on experience with messy data (e.g., electronic health records, outcomes data) and analytical methodologies
  • 5+ years working with life science/pharmaceutical/biotechnology organizations and familiarity with providing analytic services to these groups
  • Experience designing and executing research studies for life sciences
  • Strong familiarity with health data analytics tools, especially SQL, Python, R
  • Familiarity with clinical datasets and coding systems such as ICD, CPT, and RxNorm
  • Familiarity with pharmaceutical industry’s strategy and business processes, including clinical trials, new drug introduction and clinical operations
  • Ability to work effectively with cross-functional teams
  • Clear communication skills and able to deliver internal/external presentations
  • Ability to prioritize and manage multiple projects with high attention to detail

Responsibilities

  • Be a hands-on individual contributor on the Quantitative Sciences team with a solid grasp of relevant technical approaches (biostatistics and/or epidemiology) and their respective assumptions
  • Have a strong familiarity with designing analyses using observational data to ensure robust conclusions can be made
  • Direct experience working with teams embedded with life science organizations (e.g., HEOR, medical affairs, commercial)
  • Work on commercial retrospective clinical studies leveraging EHR real-world data through responsibilities such as creation of statistical analysis plans, implementation of analyses, development of algorithms in support of research objectives, and/or writing of publications
  • Collaborate with customers to understand project objectives and stakeholder needs
  • Collaborate cross-functionally with teams (e.g., Commercial/Sales, Product, Medical, Engineering/Technology, etc.) to translate clinical investigation questions into detailed data analytics requirements for internal and external projects
  • Provide technical leadership by leading projects, conducting comprehensive code reviews, and ensuring a deep understanding of code and its implications for data analysis and research objectives

Preferred Qualifications

  • Direct experience working with ophthalmology, urology, and/or neurology clinical data is considered a plus