Principal Biostatistician

4 weeks ago


Wilmington, United States Talent Groups Full time

• Excellent understanding of the statistical principles underlying clinical trials

• Excellent statistical skills

• Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submission process

• Great consultative skills

• Outstanding SAS® programming skills and familiarity of other statistical packages (eg StatXact, Nquery) and understanding of database structures

• Excellent organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects

• Capable of adapting and adjusting to changing priorities

• Excellent written and verbal communication skills, including proficiency in the English language

• Capable of working in a multi-disciplinary team setting

• Demonstrated initiative, motivation and problem-solving skills

• Positive attitude and the ability to organize a team and work well with others

• Good mentoring skills as shown by leadership of multiple projects and team members



  • Wilmington, United States Inctye Full time

    Overview: Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health...


  • Wilmington, United States Incyte Full time

    Overview Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health...


  • Wilmington, United States Talent Groups Full time

    • Excellent understanding of the statistical principles underlying clinical trials • Excellent statistical skills • Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submission process • Great consultative skills • Outstanding SAS® programming skills and familiarity of other statistical packages...