A company is looking for a Principal Biostatistician who provides statistical input into clinical trial development and analysis.
Key Responsibilities
Provide statistical input into Phase I - IV clinical trial development
Analyze clinical trial data and contribute to the reporting of results
Function independently as a lead statistician on clinical trials
Required Qualifications
PhD in Statistics, Biostatistics, or related field with 5 years of experience, or a Master's degree with 8 years of experience in biostatistics
Experience in clinical trials or health research environment
Familiarity with statistical software such as SAS or SPSS
Proficiency in Microsoft Word and Excel
Ability to manage multiple tasks under tight timelines
Biostatistician • Toms River, New Jersey, United States