Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use
Job Summary
Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use.
Provides guidance and management to statisticians to ensure high quality and timely deliverables.
Effectively engages as a matrix team member on high level development teams, to act as a scientific and strategic partner in the drug development process.
Matching Summary
Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use.
Salary
Base: $244,990 - $296,867 (Cambridge Crossing); $218,740 - $265,060 (Princeton - NJ - US); Bonus/Equity: Additional incentive cash and stock opportunities (based on eligibility); Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits
Skills & Requirements
Must-have
Drug Development experience
Oncology experience
late phase clinical trials
scientific and strategic partner
regulatory agencies and industry standards
global regulatory agency interactions
Nice-to-have
innovative and efficient study design
high quality and timely deliverables
culture of inclusiveness
employee advocate and management coach
statistical community of practice
Key Requirements
PhD (9+ years experience) or MS (11+ years experience)
statistics or biostatistics or related scientific field
clinical trials, drug development, pharmaceutical industry or healthcare experience
Proficiency in scientific computing/programming (SAS, R or Python)
at least 3 years management (direct or matrix) experience is preferred