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  • Provides statistical design, analysis and interpretation of Phase 1-4 clinical trials including biomarker analyses and integrated analyses across trials
  • Actively contributes to study teams as a core member
  • Partners with Data Management, SAS Programmers, Clinical and Monitoring to ensure high quality data sets
  • Programs analysis datasets (ADaM) and TFL using SAS or other software for conferences, publications, safety reviews and regulatory requests
  • Researches and programs statistical methodologies such as Bayesian approaches, interim analyses including futility
  • Adaptimmune is a company that values the role of statisticians in making data driven decision.  Therefore, this role requires at least 50% SAS/R programming as well as statistical knowledge and experience.



  • Master’s degree in Biostatistics or Statistics with a minimum of 3 years in a pharma/ biotech/ CRO industry
  • Experience writing the statistical methods sections of protocols, statistical analysis plans, SAS programming to produce tables, listings and figures; graphics in R is acceptable.
  • Experience inputting into eCRFs, edit checks, supporting data cleaning efforts as a statistician in partnership with data management; experience QCing datasets, programming and outputs.
  • Experience working in a fast paced environment that requires ad hoc tables listings in figures on a regular basis
  • Extensive knowledge of SAS Graphics, Statistics and Base procedures and other programming languages
  • High attention to detail and strong organizational skills, planning and time-management skills.
  • Ability to manage multiple tasks against tight deadlines, maintain highly confidential and sensitive information.
  • Motivated, with high energy and strong work ethic.
  • Excellent written and verbal communication skills
  • Ability to adapt effectively to changing priorities
  • Demonstrates strong project management, teamwork, and interpersonal skills.
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