October 15
• This permanent, remote opportunity can be worked from anywhere in the U.S. • Lead large global or major projects and analyze parts of clinical studies • Provide planning on multiple clinical studies including tracking project activities • Provide statistical input into interdepartmental activities and processes • Supervise and train less experienced biostatisticians • Responsible for the development of Statistical Analysis Plans and data handling rules
• Recommended: Master's degree in Biostatistics or related field • Required: Bachelor's degree in Biostatistics or related field • Minimum Required: 5-8 years of experience or equivalent combination of education or experience • Needs minimum 2 years of Oncology experience across Phase I, II, III • Experience with Survival Analysis and stat lead experience for NDA submission studies • Ability to program in one or more statistical software packages (SAS®) • SAS proficiency including various statistical procedures • Ability to effectively communicate statistical concepts • Good knowledge of the overall clinical trial process • Experience in preparing Statistical Analysis Plans, reporting, etc.
• Medical • Dental • Vision • Life • STD/LTD • 401(K) • ESPP • Paid time off (PTO) or Flexible time off (FTO) • Company bonus where applicable
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