Associate Director, Biostatistics
$162,600–$212,600 year
Remote · United States
Job Summary
Lead the statistical support for hematology clinical studies, developing and implementing the statistical analysis plan (SAP) for the clinical study report (CSR) and regulatory submissions; collaborate with cross-functional teams to review data, design study protocols and SAPs, and analyze data to meet study objectives; prepare reports and respond to queries from clinical monitors, regulatory agencies, and investigators; contribute to manuscripts and presentations and participate in innovative statistical methods for trial development. Requires a PhD in Statistics or related field with 5+ years (or a Master’s with 8+ years) in clinical drug development; proficiency in SAS and/or R; strong communication and collaboration skills; oncology experience preferred but not required.
Required Qualifications
- PhD in Statistics or related field with 5+ years of experience, or a Master’s degree with a minimum of 8 years of experience in clinical drug development
- Experience with clinical trials and knowledge of regulatory guidance is required
- SAS and/or R proficiency strongly desirable
- Oncology experience is preferred but not required
- Excellent written and oral communication skills; ability to work in a team and independently
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